Canonical Allele Identifier: CA2643305862

Gene: MTHFR

Linked Data

• gnomAD v4: 1-11805768-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11805768A>T , CM000663.2:g.11805768A>T	GRCh38
NC_000001.10:g.11865825A>T , CM000663.1:g.11865825A>T	GRCh37
NC_000001.9:g.11788412A>T	NCBI36
NG_008766.1:g.4619A>T
NG_013351.1:g.5336T>A , LRG_726:g.5336T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.-11+120T>A	ENSP00000365669.3:n.-11+120T>A
ENST00000376590.9:c.-14+120T>A MANE Select	ENSP00000365775.3:n.-14+120T>A
ENST00000641437.1:n.119+120T>A
ENST00000641446.1:c.-14+120T>A	ENSP00000493262.1:n.-14+120T>A
ENST00000641747.1:c.-14+120T>A	ENSP00000493116.1:n.-14+120T>A
ENST00000642002.1:n.216+120T>A
ENST00000376486.2:c.-14+120T>A	ENSP00000365669.2:n.-14+120T>A
ENST00000376590.7:c.-14+120T>A	ENSP00000365775.3:n.-14+120T>A
ENST00000418034.1:c.-435T>A	ENSP00000405082.1:n.-435T>A
NM_005957.4:c.-14+120T>A , LRG_726t1:c.-14+120T>A	NP_005948.3:n.-14+120T>A
XM_005263460.3:c.-435T>A	XP_005263517.1:n.-435T>A
XM_005263461.3:c.-432T>A	XP_005263518.1:n.-432T>A
XM_005263462.3:c.-11+120T>A	XP_005263519.1:n.-11+120T>A
XM_005263463.2:c.-277+120T>A	XP_005263520.1:n.-277+120T>A
XM_005263460.5:c.-435T>A	XP_005263517.1:n.-435T>A
XM_005263462.4:c.-11+120T>A	XP_005263519.1:n.-11+120T>A
XM_005263463.4:c.-277+120T>A	XP_005263520.1:n.-277+120T>A
NM_005957.5:c.-14+120T>A MANE Select	NP_005948.3:n.-14+120T>A