Canonical Allele Identifier: CA1153799855

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794761G= , CM000663.2:g.11794761G=	GRCh38
NC_000001.10:g.11854818G= , CM000663.1:g.11854818G=	GRCh37
NC_000001.9:g.11777405G=	NCBI36
NG_013351.1:g.16343C= , LRG_726:g.16343C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1257C=	ENSP00000365770.1:p.Thr419=
ENST00000376590.9:c.1134C= MANE Select	ENSP00000365775.3:p.Thr378=
ENST00000376592.6:c.1134C=	ENSP00000365777.1:p.Thr378=
ENST00000423400.7:c.1254C=	ENSP00000398908.3:p.Thr418=
ENST00000641407.1:c.1134C=	ENSP00000493098.1:p.Thr378=
ENST00000641446.1:c.1134C=	ENSP00000493262.1:p.Thr378=
ENST00000641747.1:c.*646C=	ENSP00000493116.1:n.*646C=
ENST00000641759.1:n.1503C=
ENST00000641805.1:n.1651C=
ENST00000641820.1:c.399C=	ENSP00000492937.1:p.Thr133=
ENST00000376583.7:c.1257C=	ENSP00000365767.3:p.Thr419=
ENST00000376585.5:c.1257C=	ENSP00000365770.1:p.Thr419=
ENST00000376590.7:c.1134C=	ENSP00000365775.3:p.Thr378=
ENST00000376592.5:c.1134C=	ENSP00000365777.1:p.Thr378=
NM_005957.4:c.1134C= , LRG_726t1:c.1134C=	NP_005948.3:p.Thr378=
XM_005263458.2:c.1257C=	XP_005263515.1:p.Thr419=
XM_005263460.3:c.1134C=	XP_005263517.1:p.Thr378=
XM_005263461.3:c.1134C=	XP_005263518.1:p.Thr378=
XM_005263462.3:c.1134C=	XP_005263519.1:p.Thr378=
XM_005263463.2:c.888C=	XP_005263520.1:p.Thr296=
XM_011541495.1:c.1254C=	XP_011539797.1:p.Thr418=
XM_011541496.1:c.1257C=	XP_011539798.1:p.Thr419=
NM_001330358.1:c.1257C=	NP_001317287.1:p.Thr419=
XM_005263460.5:c.1134C=	XP_005263517.1:p.Thr378=
XM_005263462.4:c.1134C=	XP_005263519.1:p.Thr378=
XM_005263463.4:c.888C=	XP_005263520.1:p.Thr296=
XM_011541495.3:c.1254C=	XP_011539797.1:p.Thr418=
XM_011541496.3:c.1257C=	XP_011539798.1:p.Thr419=
XM_017001328.2:c.1257C=	XP_016856817.1:p.Thr419=
XM_024447198.1:c.888C=	XP_024302966.1:p.Thr296=
XR_002956640.1:n.2235C=
NM_005957.5:c.1134C= MANE Select	NP_005948.3:p.Thr378=
NM_001330358.2:c.1257C=	NP_001317287.1:p.Thr419=