Canonical Allele Identifier: CA1141826707

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790418C= , CM000663.2:g.11790418C=	GRCh38
NC_000001.10:g.11850475C= , CM000663.1:g.11850475C=	GRCh37
NC_000001.9:g.11773062C=	NCBI36
NG_013351.1:g.20686G= , LRG_726:g.20686G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.*262G=	ENSP00000365770.1:n.*262G=
ENST00000376590.9:c.*262G= MANE Select	ENSP00000365775.3:n.*262G=
ENST00000376592.6:c.*262G=	ENSP00000365777.1:n.*262G=
ENST00000423400.7:c.*262G=	ENSP00000398908.3:n.*262G=
ENST00000641407.1:c.*122G=	ENSP00000493098.1:n.*122G=
ENST00000641446.1:c.*692G=	ENSP00000493262.1:n.*692G=
ENST00000641747.1:c.*1745G=	ENSP00000493116.1:n.*1745G=
ENST00000641805.1:n.2568G=
ENST00000376583.7:c.2356G=	ENSP00000365767.3:n.2356G=
ENST00000376585.5:c.*262G=	ENSP00000365770.1:n.*262G=
ENST00000376590.7:c.*262G=	ENSP00000365775.3:n.*262G=
ENST00000376592.5:c.*262G=	ENSP00000365777.1:n.*262G=
NM_005957.4:c.*262G= , LRG_726t1:c.*262G=	NP_005948.3:n.*262G=
XM_005263458.2:c.*262G=	XP_005263515.1:n.*262G=
XM_005263460.3:c.*262G=	XP_005263517.1:n.*262G=
XM_005263461.3:c.*262G=	XP_005263518.1:n.*262G=
XM_005263462.3:c.*262G=	XP_005263519.1:n.*262G=
XM_005263463.2:c.*262G=	XP_005263520.1:n.*262G=
XM_011541495.1:c.*262G=	XP_011539797.1:n.*262G=
XM_011541496.1:c.*122G=	XP_011539798.1:n.*122G=
NM_001330358.1:c.*262G=	NP_001317287.1:n.*262G=
XM_005263460.5:c.*262G=	XP_005263517.1:n.*262G=
XM_005263462.4:c.*262G=	XP_005263519.1:n.*262G=
XM_005263463.4:c.*262G=	XP_005263520.1:n.*262G=
XM_011541495.3:c.*262G=	XP_011539797.1:n.*262G=
XM_011541496.3:c.*122G=	XP_011539798.1:n.*122G=
XM_024447198.1:c.*262G=	XP_024302966.1:n.*262G=
NM_005957.5:c.*262G= MANE Select	NP_005948.3:n.*262G=
NM_001330358.2:c.*262G=	NP_001317287.1:n.*262G=