Canonical Allele Identifier: CA1153814739

Gene: MTHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11805656C= , CM000663.2:g.11805656C=	GRCh38
NC_000001.10:g.11865713C= , CM000663.1:g.11865713C=	GRCh37
NC_000001.9:g.11788300C=	NCBI36
NG_008766.1:g.4507C=
NG_013351.1:g.5448G= , LRG_726:g.5448G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.-11+232G=	ENSP00000365669.3:n.-11+232G=
ENST00000376590.9:c.-14+232G= MANE Select	ENSP00000365775.3:n.-14+232G=
ENST00000641437.1:n.119+232G=
ENST00000641446.1:c.-14+232G=	ENSP00000493262.1:n.-14+232G=
ENST00000641747.1:c.-14+232G=	ENSP00000493116.1:n.-14+232G=
ENST00000642002.1:n.216+232G=
ENST00000376486.2:c.-14+232G=	ENSP00000365669.2:n.-14+232G=
ENST00000376590.7:c.-14+232G=	ENSP00000365775.3:n.-14+232G=
ENST00000418034.1:c.-323G=	ENSP00000405082.1:n.-323G=
NM_005957.4:c.-14+232G= , LRG_726t1:c.-14+232G=	NP_005948.3:n.-14+232G=
XM_005263460.3:c.-323G=	XP_005263517.1:n.-323G=
XM_005263461.3:c.-320G=	XP_005263518.1:n.-320G=
XM_005263462.3:c.-11+232G=	XP_005263519.1:n.-11+232G=
XM_005263463.2:c.-277+232G=	XP_005263520.1:n.-277+232G=
XM_005263460.5:c.-323G=	XP_005263517.1:n.-323G=
XM_005263462.4:c.-11+232G=	XP_005263519.1:n.-11+232G=
XM_005263463.4:c.-277+232G=	XP_005263520.1:n.-277+232G=
NM_005957.5:c.-14+232G= MANE Select	NP_005948.3:n.-14+232G=