Canonical Allele Identifier: CA1141440653

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790890G= , CM000663.2:g.11790890G=	GRCh38
NC_000001.10:g.11850947G= , CM000663.1:g.11850947G=	GRCh37
NC_000001.9:g.11773534G=	NCBI36
NG_013351.1:g.20214C= , LRG_726:g.20214C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1884C=	ENSP00000365770.1:p.Ala628=
ENST00000376590.9:c.1761C= MANE Select	ENSP00000365775.3:p.Ala587=
ENST00000376592.6:c.1761C=	ENSP00000365777.1:p.Ala587=
ENST00000423400.7:c.1881C=	ENSP00000398908.3:p.Ala627=
ENST00000641407.1:c.1753-174C=	ENSP00000493098.1:n.1753-174C=
ENST00000641446.1:c.*220C=	ENSP00000493262.1:n.*220C=
ENST00000641747.1:c.*1273C=	ENSP00000493116.1:n.*1273C=
ENST00000641759.1:n.2130C=
ENST00000641805.1:n.2270-174C=
ENST00000641820.1:c.1026C=	ENSP00000492937.1:p.Ala342=
ENST00000376583.7:c.1884C=	ENSP00000365767.3:p.Ala628=
ENST00000376585.5:c.1884C=	ENSP00000365770.1:p.Ala628=
ENST00000376590.7:c.1761C=	ENSP00000365775.3:p.Ala587=
ENST00000376592.5:c.1761C=	ENSP00000365777.1:p.Ala587=
NM_005957.4:c.1761C= , LRG_726t1:c.1761C=	NP_005948.3:p.Ala587=
XM_005263458.2:c.1884C=	XP_005263515.1:p.Ala628=
XM_005263460.3:c.1761C=	XP_005263517.1:p.Ala587=
XM_005263461.3:c.1761C=	XP_005263518.1:p.Ala587=
XM_005263462.3:c.1761C=	XP_005263519.1:p.Ala587=
XM_005263463.2:c.1515C=	XP_005263520.1:p.Ala505=
XM_011541495.1:c.1881C=	XP_011539797.1:p.Ala627=
XM_011541496.1:c.1876-174C=	XP_011539798.1:n.1876-174C=
NM_001330358.1:c.1884C=	NP_001317287.1:p.Ala628=
XM_005263460.5:c.1761C=	XP_005263517.1:p.Ala587=
XM_005263462.4:c.1761C=	XP_005263519.1:p.Ala587=
XM_005263463.4:c.1515C=	XP_005263520.1:p.Ala505=
XM_011541495.3:c.1881C=	XP_011539797.1:p.Ala627=
XM_011541496.3:c.1876-174C=	XP_011539798.1:n.1876-174C=
XM_017001328.2:c.1876-142C=	XP_016856817.1:n.1876-142C=
XM_024447198.1:c.1515C=	XP_024302966.1:p.Ala505=
XR_002956640.1:n.2854-174C=
NM_005957.5:c.1761C= MANE Select	NP_005948.3:p.Ala587=
NM_001330358.2:c.1884C=	NP_001317287.1:p.Ala628=