Canonical Allele Identifier: CA1153786255
Gene: C1orf167 HGNC NCBI
MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11787771_11787781delinsTTCCTCCACCC , CM000663.2:g.11787771_11787781delinsTTCCTCCACCC GRCh38
NC_000001.10:g.11847828_11847838delinsTTCCTCCACCC , CM000663.1:g.11847828_11847838delinsTTCCTCCACCC GRCh37
NC_000001.9:g.11770415_11770425delinsTTCCTCCACCC NCBI36
NG_013351.1:g.23323_23333delinsGGGTGGAGGAA , LRG_726:g.23323_23333delinsGGGTGGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000433342.6:c.3188-102_3188-92delinsTTCCTCCACCC (C1orf167) ENSP00000414909.3:n.3188-102_3188-92delinsTTCCTCCACCC
ENST00000688073.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) MANE Select ENSP00000510540.1:n.3674-102_3674-92delinsTTCCTCCACCC
ENST00000376585.6:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) ENSP00000365770.1:n.*2899_*2909delinsGGGTGGAGGAA
ENST00000376590.9:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) MANE Select ENSP00000365775.3:n.*2899_*2909delinsGGGTGGAGGAA
ENST00000376592.6:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) ENSP00000365777.1:n.*2899_*2909delinsGGGTGGAGGAA
ENST00000312793.9:c.1824-102_1824-92delinsTTCCTCCACCC (C1orf167)
ENST00000376583.7:c.4993_5003delinsGGGTGGAGGAA (MTHFR) ENSP00000365767.3:n.4993_5003delinsGGGTGGAGGAA
ENST00000376590.7:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) ENSP00000365775.3:n.*2899_*2909delinsGGGTGGAGGAA
ENST00000376592.5:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) ENSP00000365777.1:n.*2899_*2909delinsGGGTGGAGGAA
ENST00000433342.5:c.3746-102_3746-92delinsTTCCTCCACCC (C1orf167) ENSP00000414909.2:n.3746-102_3746-92delinsTTCCTCCACCC
ENST00000444493.5:c.1173-102_1173-92delinsTTCCTCCACCC (C1orf167)
ENST00000449278.1:c.1003-102_1003-92delinsTTCCTCCACCC (C1orf167)
ENST00000475041.1:n.503_513delinsTTCCTCCACCC (C1orf167)
NM_001010881.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) NP_001010881.1:n.3674-102_3674-92delinsTTCCTCCACCC
NM_005957.4:c.*2899_*2909delinsGGGTGGAGGAA , LRG_726t1:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) NP_005948.3:n.*2899_*2909delinsGGGTGGAGGAA
XM_006711078.2:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_006711141.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_011541267.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539569.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541268.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539570.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541269.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539571.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541270.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539572.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541271.1:c.3755-102_3755-92delinsTTCCTCCACCC (C1orf167) XP_011539573.1:n.3755-102_3755-92delinsTTCCTCCACCC
XM_011541272.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539574.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541273.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_011539575.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_011541274.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_011539576.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_011541275.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_011539577.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_011541276.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539578.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541277.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539579.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541278.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539580.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541279.1:c.3401-102_3401-92delinsTTCCTCCACCC (C1orf167) XP_011539581.1:n.3401-102_3401-92delinsTTCCTCCACCC
XM_011541280.1:c.2090-102_2090-92delinsTTCCTCCACCC (C1orf167) XP_011539582.1:n.2090-102_2090-92delinsTTCCTCCACCC
XM_011541281.1:c.2090-102_2090-92delinsTTCCTCCACCC (C1orf167) XP_011539583.1:n.2090-102_2090-92delinsTTCCTCCACCC
NM_001330358.1:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) NP_001317287.1:n.*2899_*2909delinsGGGTGGAGGAA
XM_011541272.3:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539574.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541276.3:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539578.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541277.3:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539579.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_011541278.2:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_011539580.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_024446506.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_024302274.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_024446507.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_024302275.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_024446508.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_024302276.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_024446509.1:c.3809-102_3809-92delinsTTCCTCCACCC (C1orf167) XP_024302277.1:n.3809-102_3809-92delinsTTCCTCCACCC
XM_024446512.1:c.3755-102_3755-92delinsTTCCTCCACCC (C1orf167) XP_024302280.1:n.3755-102_3755-92delinsTTCCTCCACCC
XM_024446514.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_024302282.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_024446515.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_024302283.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_024446517.1:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) XP_024302285.1:n.3674-102_3674-92delinsTTCCTCCACCC
XM_024446518.1:c.2090-102_2090-92delinsTTCCTCCACCC (C1orf167) XP_024302286.1:n.2090-102_2090-92delinsTTCCTCCACCC
NM_001010881.2:c.3674-102_3674-92delinsTTCCTCCACCC (C1orf167) MANE Select NP_001010881.1:n.3674-102_3674-92delinsTTCCTCCACCC
NM_005957.5:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) MANE Select NP_005948.3:n.*2899_*2909delinsGGGTGGAGGAA
NM_001330358.2:c.*2899_*2909delinsGGGTGGAGGAA (MTHFR) NP_001317287.1:n.*2899_*2909delinsGGGTGGAGGAA