Canonical Allele Identifier: CA1153810844

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11800273T= , CM000663.2:g.11800273T=	GRCh38
NC_000001.10:g.11860330T= , CM000663.1:g.11860330T=	GRCh37
NC_000001.9:g.11782917T=	NCBI36
NG_013351.1:g.10831A= , LRG_726:g.10831A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.525A=	ENSP00000365669.3:p.Ala175=
ENST00000376585.6:c.648A=	ENSP00000365770.1:p.Ala216=
ENST00000376590.9:c.525A= MANE Select	ENSP00000365775.3:p.Ala175=
ENST00000376592.6:c.525A=	ENSP00000365777.1:p.Ala175=
ENST00000423400.7:c.645A=	ENSP00000398908.3:p.Ala215=
ENST00000641407.1:c.525A=	ENSP00000493098.1:p.Ala175=
ENST00000641437.1:n.1495A=
ENST00000641446.1:c.525A=	ENSP00000493262.1:p.Ala175=
ENST00000641721.1:n.582A=
ENST00000641747.1:c.*37A=	ENSP00000493116.1:n.*37A=
ENST00000641759.1:n.660A=
ENST00000641805.1:n.808A=
ENST00000641909.1:n.1773A=
ENST00000376583.7:c.648A=	ENSP00000365767.3:p.Ala216=
ENST00000376585.5:c.648A=	ENSP00000365770.1:p.Ala216=
ENST00000376590.7:c.525A=	ENSP00000365775.3:p.Ala175=
ENST00000376592.5:c.525A=	ENSP00000365777.1:p.Ala175=
NM_005957.4:c.525A= , LRG_726t1:c.525A=	NP_005948.3:p.Ala175=
XM_005263458.2:c.648A=	XP_005263515.1:p.Ala216=
XM_005263460.3:c.525A=	XP_005263517.1:p.Ala175=
XM_005263461.3:c.525A=	XP_005263518.1:p.Ala175=
XM_005263462.3:c.525A=	XP_005263519.1:p.Ala175=
XM_005263463.2:c.279A=	XP_005263520.1:p.Ala93=
XM_011541495.1:c.645A=	XP_011539797.1:p.Ala215=
XM_011541496.1:c.648A=	XP_011539798.1:p.Ala216=
NM_001330358.1:c.648A=	NP_001317287.1:p.Ala216=
XM_005263460.5:c.525A=	XP_005263517.1:p.Ala175=
XM_005263462.4:c.525A=	XP_005263519.1:p.Ala175=
XM_005263463.4:c.279A=	XP_005263520.1:p.Ala93=
XM_011541495.3:c.645A=	XP_011539797.1:p.Ala215=
XM_011541496.3:c.648A=	XP_011539798.1:p.Ala216=
XM_017001328.2:c.648A=	XP_016856817.1:p.Ala216=
XM_024447198.1:c.279A=	XP_024302966.1:p.Ala93=
XR_002956640.1:n.1392A=
NM_005957.5:c.525A= MANE Select	NP_005948.3:p.Ala175=
NM_001330358.2:c.648A=	NP_001317287.1:p.Ala216=