Canonical Allele Identifier: CA1153803228

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796223C= , CM000663.2:g.11796223C=	GRCh38
NC_000001.10:g.11856280C= , CM000663.1:g.11856280C=	GRCh37
NC_000001.9:g.11778867C=	NCBI36
NG_013351.1:g.14881G= , LRG_726:g.14881G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.886G=	ENSP00000365770.1:p.Gly296=
ENST00000376590.9:c.763G= MANE Select	ENSP00000365775.3:p.Gly255=
ENST00000376592.6:c.763G=	ENSP00000365777.1:p.Gly255=
ENST00000423400.7:c.883G=	ENSP00000398908.3:p.Gly295=
ENST00000641407.1:c.763G=	ENSP00000493098.1:p.Gly255=
ENST00000641446.1:c.763G=	ENSP00000493262.1:p.Gly255=
ENST00000641721.1:n.644-875G=
ENST00000641747.1:c.*275G=	ENSP00000493116.1:n.*275G=
ENST00000641759.1:n.898G=
ENST00000641805.1:n.1046G=
ENST00000641820.1:c.28G=	ENSP00000492937.1:p.Gly10=
ENST00000376583.7:c.886G=	ENSP00000365767.3:p.Gly296=
ENST00000376585.5:c.886G=	ENSP00000365770.1:p.Gly296=
ENST00000376590.7:c.763G=	ENSP00000365775.3:p.Gly255=
ENST00000376592.5:c.763G=	ENSP00000365777.1:p.Gly255=
NM_005957.4:c.763G= , LRG_726t1:c.763G=	NP_005948.3:p.Gly255=
XM_005263458.2:c.886G=	XP_005263515.1:p.Gly296=
XM_005263460.3:c.763G=	XP_005263517.1:p.Gly255=
XM_005263461.3:c.763G=	XP_005263518.1:p.Gly255=
XM_005263462.3:c.763G=	XP_005263519.1:p.Gly255=
XM_005263463.2:c.517G=	XP_005263520.1:p.Gly173=
XM_011541495.1:c.883G=	XP_011539797.1:p.Gly295=
XM_011541496.1:c.886G=	XP_011539798.1:p.Gly296=
NM_001330358.1:c.886G=	NP_001317287.1:p.Gly296=
XM_005263460.5:c.763G=	XP_005263517.1:p.Gly255=
XM_005263462.4:c.763G=	XP_005263519.1:p.Gly255=
XM_005263463.4:c.517G=	XP_005263520.1:p.Gly173=
XM_011541495.3:c.883G=	XP_011539797.1:p.Gly295=
XM_011541496.3:c.886G=	XP_011539798.1:p.Gly296=
XM_017001328.2:c.886G=	XP_016856817.1:p.Gly296=
XM_024447198.1:c.517G=	XP_024302966.1:p.Gly173=
XR_002956640.1:n.1630G=
NM_005957.5:c.763G= MANE Select	NP_005948.3:p.Gly255=
NM_001330358.2:c.886G=	NP_001317287.1:p.Gly296=