Canonical Allele Identifier: CA2572365536
Gene: C1orf167 HGNC NCBI
MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11788196_11788197insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA , CM000663.2:g.11788196_11788197insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA GRCh38
NC_000001.10:g.11848253_11848254insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA , CM000663.1:g.11848253_11848254insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA GRCh37
NC_000001.9:g.11770840_11770841insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA NCBI36
NG_013351.1:g.22907_22908insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC , LRG_726:g.22907_22908insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000433342.6:c.3395_3396insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) ENSP00000414909.3:p.Ser1133PhefsTer6
ENST00000688073.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) MANE Select ENSP00000510540.1:p.Ser1300PhefsTer6
ENST00000376585.6:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) ENSP00000365770.1:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACT...
ENST00000376590.9:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) MANE Select ENSP00000365775.3:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACT...
ENST00000376592.6:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) ENSP00000365777.1:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACT...
ENST00000312793.9:c.2031_2032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167)
ENST00000376583.7:c.4577_4578insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) ENSP00000365767.3:n.4577_4578insTTCAGAGTTGCTTGTCAGAGGCTGACTGA...
ENST00000376590.7:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) ENSP00000365775.3:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACT...
ENST00000376592.5:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) ENSP00000365777.1:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACT...
ENST00000433342.5:c.3953_3954insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) ENSP00000414909.2:p.Ser1319PhefsTer6
ENST00000444493.5:c.1395_1396insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167)
ENST00000449278.1:c.1178-47_1178-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167)
ENST00000482358.1:n.237-47_237-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167)
NM_001010881.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) NP_001010881.1:p.Ser1300PhefsTer6
NM_005957.4:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC , LRG_726t1:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) NP_005948.3:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC...
XM_006711078.2:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_006711141.1:p.Ser1300PhefsTer6
XM_011541267.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539569.1:p.Ser1345PhefsTer6
XM_011541268.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539570.1:p.Ser1345PhefsTer6
XM_011541269.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539571.1:p.Ser1345PhefsTer6
XM_011541270.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539572.1:p.Ser1345PhefsTer6
XM_011541271.1:c.3977_3978insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539573.1:p.Ser1327PhefsTer6
XM_011541272.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539574.1:p.Ser1345PhefsTer6
XM_011541273.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539575.1:p.Ser1300PhefsTer6
XM_011541274.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539576.1:p.Ser1300PhefsTer6
XM_011541275.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539577.1:p.Ser1300PhefsTer6
XM_011541276.1:c.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539578.1:n.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAA...
XM_011541277.1:c.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539579.1:n.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAA...
XM_011541278.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539580.1:p.Ser1345PhefsTer6
XM_011541279.1:c.3623_3624insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539581.1:p.Ser1209PhefsTer6
XM_011541280.1:c.2312_2313insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539582.1:p.Ser772PhefsTer6
XM_011541281.1:c.2312_2313insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539583.1:p.Ser772PhefsTer6
NM_001330358.1:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) NP_001317287.1:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAG...
XM_011541272.3:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539574.1:p.Ser1345PhefsTer6
XM_011541276.3:c.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539578.1:n.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAA...
XM_011541277.3:c.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539579.1:n.3984-47_3984-46insGTTCTCAGTCAGCCTCTGACAAGCAA...
XM_011541278.2:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_011539580.1:p.Ser1345PhefsTer6
XM_024446506.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302274.1:p.Ser1345PhefsTer6
XM_024446507.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302275.1:p.Ser1345PhefsTer6
XM_024446508.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302276.1:p.Ser1345PhefsTer6
XM_024446509.1:c.4031_4032insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302277.1:p.Ser1345PhefsTer6
XM_024446512.1:c.3977_3978insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302280.1:p.Ser1327PhefsTer6
XM_024446514.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302282.1:p.Ser1300PhefsTer6
XM_024446515.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302283.1:p.Ser1300PhefsTer6
XM_024446517.1:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302285.1:p.Ser1300PhefsTer6
XM_024446518.1:c.2312_2313insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) XP_024302286.1:p.Ser772PhefsTer6
NM_001010881.2:c.3896_3897insGTTCTCAGTCAGCCTCTGACAAGCAACTCTGAA (C1orf167) MANE Select NP_001010881.1:p.Ser1300PhefsTer6
NM_005957.5:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) MANE Select NP_005948.3:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC...
NM_001330358.2:c.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAGAAC (MTHFR) NP_001317287.1:n.*2483_*2484insTTCAGAGTTGCTTGTCAGAGGCTGACTGAG...