Canonical Allele Identifier: CA1142166249
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11801299C= , CM000663.2:g.11801299C= GRCh38
NC_000001.10:g.11861356C= , CM000663.1:g.11861356C= GRCh37
NC_000001.9:g.11783943C= NCBI36
NG_008766.1:g.150C=
NG_013351.1:g.9805G= , LRG_726:g.9805G=

Transcript Alleles

HGVS Amino-acid Change
NM_005957.5:c.337G= MANE Select NP_005948.3:p.Ala113=
ENST00000376590.9:c.337G= MANE Select ENSP00000365775.3:p.Ala113=
NM_001330358.1:c.460G= NP_001317287.1:p.Ala154=
NM_001330358.2:c.460G= NP_001317287.1:p.Ala154=
NM_005957.4:c.337G= , LRG_726t1:c.337G= NP_005948.3:p.Ala113=
ENST00000376486.3:c.337G= ENSP00000365669.3:p.Ala113=
ENST00000376583.7:c.460G= ENSP00000365767.3:p.Ala154=
ENST00000376585.5:c.460G= ENSP00000365770.1:p.Ala154=
ENST00000376585.6:c.460G= ENSP00000365770.1:p.Ala154=
ENST00000376590.7:c.337G= ENSP00000365775.3:p.Ala113=
ENST00000376592.5:c.337G= ENSP00000365777.1:p.Ala113=
ENST00000376592.6:c.337G= ENSP00000365777.1:p.Ala113=
ENST00000418034.1:c.337G= ENSP00000405082.1:p.Ala113=
ENST00000423400.7:c.457G= ENSP00000398908.3:p.Ala153=
ENST00000641407.1:c.337G= ENSP00000493098.1:p.Ala113=
ENST00000641437.1:n.469G=
ENST00000641446.1:c.337G= ENSP00000493262.1:p.Ala113=
ENST00000641721.1:n.394G=
ENST00000641747.1:c.237-977G= ENSP00000493116.1:n.237-977G=
ENST00000641759.1:n.472G=
ENST00000641805.1:n.620G=
ENST00000641909.1:n.747G=
XM_005263458.2:c.460G= XP_005263515.1:p.Ala154=
XM_005263460.3:c.337G= XP_005263517.1:p.Ala113=
XM_005263460.5:c.337G= XP_005263517.1:p.Ala113=
XM_005263461.3:c.337G= XP_005263518.1:p.Ala113=
XM_005263462.3:c.337G= XP_005263519.1:p.Ala113=
XM_005263462.4:c.337G= XP_005263519.1:p.Ala113=
XM_005263463.2:c.91G= XP_005263520.1:p.Ala31=
XM_005263463.4:c.91G= XP_005263520.1:p.Ala31=
XM_011541495.1:c.457G= XP_011539797.1:p.Ala153=
XM_011541495.3:c.457G= XP_011539797.1:p.Ala153=
XM_011541496.1:c.460G= XP_011539798.1:p.Ala154=
XM_011541496.3:c.460G= XP_011539798.1:p.Ala154=
XM_017001328.2:c.460G= XP_016856817.1:p.Ala154=
XM_024447198.1:c.91G= XP_024302966.1:p.Ala31=
XR_002956640.1:n.1204G=