Canonical Allele Identifier: CA2643294938
Gene: C1orf167 HGNC NCBI
MTHFR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11787703_11787722del , CM000663.2:g.11787703_11787722del GRCh38
NC_000001.10:g.11847760_11847779del , CM000663.1:g.11847760_11847779del GRCh37
NC_000001.9:g.11770347_11770366del NCBI36
NG_013351.1:g.23385_23404del , LRG_726:g.23385_23404del

Transcript Alleles

HGVS Amino-acid Change
ENST00000433342.6:c.3188-170_3188-151del (C1orf167) ENSP00000414909.3:n.3188-170_3188-151del
ENST00000688073.1:c.3674-170_3674-151del (C1orf167) MANE Select ENSP00000510540.1:n.3674-170_3674-151del
ENST00000376585.6:c.*2961_*2980del (MTHFR) ENSP00000365770.1:n.*2961_*2980del
ENST00000376590.9:c.*2961_*2980del (MTHFR) MANE Select ENSP00000365775.3:n.*2961_*2980del
ENST00000376592.6:c.*2961_*2980del (MTHFR) ENSP00000365777.1:n.*2961_*2980del
ENST00000312793.9:c.1824-170_1824-151del (C1orf167)
ENST00000376583.7:c.5055_5074del (MTHFR) ENSP00000365767.3:n.5055_5074del
ENST00000376590.7:c.*2961_*2980del (MTHFR) ENSP00000365775.3:n.*2961_*2980del
ENST00000376592.5:c.*2961_*2980del (MTHFR) ENSP00000365777.1:n.*2961_*2980del
ENST00000433342.5:c.3746-170_3746-151del (C1orf167) ENSP00000414909.2:n.3746-170_3746-151del
ENST00000444493.5:c.1173-170_1173-151del (C1orf167)
ENST00000449278.1:c.1003-170_1003-151del (C1orf167)
ENST00000475041.1:n.435_454del (C1orf167)
NM_001010881.1:c.3674-170_3674-151del (C1orf167) NP_001010881.1:n.3674-170_3674-151del
NM_005957.4:c.*2961_*2980del , LRG_726t1:c.*2961_*2980del (MTHFR) NP_005948.3:n.*2961_*2980del
XM_006711078.2:c.3674-170_3674-151del (C1orf167) XP_006711141.1:n.3674-170_3674-151del
XM_011541267.1:c.3809-170_3809-151del (C1orf167) XP_011539569.1:n.3809-170_3809-151del
XM_011541268.1:c.3809-170_3809-151del (C1orf167) XP_011539570.1:n.3809-170_3809-151del
XM_011541269.1:c.3809-170_3809-151del (C1orf167) XP_011539571.1:n.3809-170_3809-151del
XM_011541270.1:c.3809-170_3809-151del (C1orf167) XP_011539572.1:n.3809-170_3809-151del
XM_011541271.1:c.3755-170_3755-151del (C1orf167) XP_011539573.1:n.3755-170_3755-151del
XM_011541272.1:c.3809-170_3809-151del (C1orf167) XP_011539574.1:n.3809-170_3809-151del
XM_011541273.1:c.3674-170_3674-151del (C1orf167) XP_011539575.1:n.3674-170_3674-151del
XM_011541274.1:c.3674-170_3674-151del (C1orf167) XP_011539576.1:n.3674-170_3674-151del
XM_011541275.1:c.3674-170_3674-151del (C1orf167) XP_011539577.1:n.3674-170_3674-151del
XM_011541276.1:c.3809-170_3809-151del (C1orf167) XP_011539578.1:n.3809-170_3809-151del
XM_011541277.1:c.3809-170_3809-151del (C1orf167) XP_011539579.1:n.3809-170_3809-151del
XM_011541278.1:c.3809-170_3809-151del (C1orf167) XP_011539580.1:n.3809-170_3809-151del
XM_011541279.1:c.3401-170_3401-151del (C1orf167) XP_011539581.1:n.3401-170_3401-151del
XM_011541280.1:c.2090-170_2090-151del (C1orf167) XP_011539582.1:n.2090-170_2090-151del
XM_011541281.1:c.2090-170_2090-151del (C1orf167) XP_011539583.1:n.2090-170_2090-151del
NM_001330358.1:c.*2961_*2980del (MTHFR) NP_001317287.1:n.*2961_*2980del
XM_011541272.3:c.3809-170_3809-151del (C1orf167) XP_011539574.1:n.3809-170_3809-151del
XM_011541276.3:c.3809-170_3809-151del (C1orf167) XP_011539578.1:n.3809-170_3809-151del
XM_011541277.3:c.3809-170_3809-151del (C1orf167) XP_011539579.1:n.3809-170_3809-151del
XM_011541278.2:c.3809-170_3809-151del (C1orf167) XP_011539580.1:n.3809-170_3809-151del
XM_024446506.1:c.3809-170_3809-151del (C1orf167) XP_024302274.1:n.3809-170_3809-151del
XM_024446507.1:c.3809-170_3809-151del (C1orf167) XP_024302275.1:n.3809-170_3809-151del
XM_024446508.1:c.3809-170_3809-151del (C1orf167) XP_024302276.1:n.3809-170_3809-151del
XM_024446509.1:c.3809-170_3809-151del (C1orf167) XP_024302277.1:n.3809-170_3809-151del
XM_024446512.1:c.3755-170_3755-151del (C1orf167) XP_024302280.1:n.3755-170_3755-151del
XM_024446514.1:c.3674-170_3674-151del (C1orf167) XP_024302282.1:n.3674-170_3674-151del
XM_024446515.1:c.3674-170_3674-151del (C1orf167) XP_024302283.1:n.3674-170_3674-151del
XM_024446517.1:c.3674-170_3674-151del (C1orf167) XP_024302285.1:n.3674-170_3674-151del
XM_024446518.1:c.2090-170_2090-151del (C1orf167) XP_024302286.1:n.2090-170_2090-151del
NM_001010881.2:c.3674-170_3674-151del (C1orf167) MANE Select NP_001010881.1:n.3674-170_3674-151del
NM_005957.5:c.*2961_*2980del (MTHFR) MANE Select NP_005948.3:n.*2961_*2980del
NM_001330358.2:c.*2961_*2980del (MTHFR) NP_001317287.1:n.*2961_*2980del
Search 100 bp 5'
Search 100 bp 3'