Canonical Allele Identifier: CA1153799706

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794732C= , CM000663.2:g.11794732C=	GRCh38
NC_000001.10:g.11854789C= , CM000663.1:g.11854789C=	GRCh37
NC_000001.9:g.11777376C=	NCBI36
NG_013351.1:g.16372G= , LRG_726:g.16372G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1286G=	ENSP00000365770.1:p.Arg429=
ENST00000376590.9:c.1163G= MANE Select	ENSP00000365775.3:p.Arg388=
ENST00000376592.6:c.1163G=	ENSP00000365777.1:p.Arg388=
ENST00000423400.7:c.1283G=	ENSP00000398908.3:p.Arg428=
ENST00000641407.1:c.1163G=	ENSP00000493098.1:p.Arg388=
ENST00000641446.1:c.1163G=	ENSP00000493262.1:p.Arg388=
ENST00000641747.1:c.*675G=	ENSP00000493116.1:n.*675G=
ENST00000641759.1:n.1532G=
ENST00000641805.1:n.1680G=
ENST00000641820.1:c.428G=	ENSP00000492937.1:p.Arg143=
ENST00000376583.7:c.1286G=	ENSP00000365767.3:p.Arg429=
ENST00000376585.5:c.1286G=	ENSP00000365770.1:p.Arg429=
ENST00000376590.7:c.1163G=	ENSP00000365775.3:p.Arg388=
ENST00000376592.5:c.1163G=	ENSP00000365777.1:p.Arg388=
NM_005957.4:c.1163G= , LRG_726t1:c.1163G=	NP_005948.3:p.Arg388=
XM_005263458.2:c.1286G=	XP_005263515.1:p.Arg429=
XM_005263460.3:c.1163G=	XP_005263517.1:p.Arg388=
XM_005263461.3:c.1163G=	XP_005263518.1:p.Arg388=
XM_005263462.3:c.1163G=	XP_005263519.1:p.Arg388=
XM_005263463.2:c.917G=	XP_005263520.1:p.Arg306=
XM_011541495.1:c.1283G=	XP_011539797.1:p.Arg428=
XM_011541496.1:c.1286G=	XP_011539798.1:p.Arg429=
NM_001330358.1:c.1286G=	NP_001317287.1:p.Arg429=
XM_005263460.5:c.1163G=	XP_005263517.1:p.Arg388=
XM_005263462.4:c.1163G=	XP_005263519.1:p.Arg388=
XM_005263463.4:c.917G=	XP_005263520.1:p.Arg306=
XM_011541495.3:c.1283G=	XP_011539797.1:p.Arg428=
XM_011541496.3:c.1286G=	XP_011539798.1:p.Arg429=
XM_017001328.2:c.1286G=	XP_016856817.1:p.Arg429=
XM_024447198.1:c.917G=	XP_024302966.1:p.Arg306=
XR_002956640.1:n.2264G=
NM_005957.5:c.1163G= MANE Select	NP_005948.3:p.Arg388=
NM_001330358.2:c.1286G=	NP_001317287.1:p.Arg429=