Canonical Allele Identifier: CA2643305334

Gene: MTHFR

Linked Data

• gnomAD v4: 1-11805657-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11805657A>G , CM000663.2:g.11805657A>G	GRCh38
NC_000001.10:g.11865714A>G , CM000663.1:g.11865714A>G	GRCh37
NC_000001.9:g.11788301A>G	NCBI36
NG_008766.1:g.4508A>G
NG_013351.1:g.5447T>C , LRG_726:g.5447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.-11+231T>C	ENSP00000365669.3:n.-11+231T>C
ENST00000376590.9:c.-14+231T>C MANE Select	ENSP00000365775.3:n.-14+231T>C
ENST00000641437.1:n.119+231T>C
ENST00000641446.1:c.-14+231T>C	ENSP00000493262.1:n.-14+231T>C
ENST00000641747.1:c.-14+231T>C	ENSP00000493116.1:n.-14+231T>C
ENST00000642002.1:n.216+231T>C
ENST00000376486.2:c.-14+231T>C	ENSP00000365669.2:n.-14+231T>C
ENST00000376590.7:c.-14+231T>C	ENSP00000365775.3:n.-14+231T>C
ENST00000418034.1:c.-324T>C	ENSP00000405082.1:n.-324T>C
NM_005957.4:c.-14+231T>C , LRG_726t1:c.-14+231T>C	NP_005948.3:n.-14+231T>C
XM_005263460.3:c.-324T>C	XP_005263517.1:n.-324T>C
XM_005263461.3:c.-321T>C	XP_005263518.1:n.-321T>C
XM_005263462.3:c.-11+231T>C	XP_005263519.1:n.-11+231T>C
XM_005263463.2:c.-277+231T>C	XP_005263520.1:n.-277+231T>C
XM_005263460.5:c.-324T>C	XP_005263517.1:n.-324T>C
XM_005263462.4:c.-11+231T>C	XP_005263519.1:n.-11+231T>C
XM_005263463.4:c.-277+231T>C	XP_005263520.1:n.-277+231T>C
NM_005957.5:c.-14+231T>C MANE Select	NP_005948.3:n.-14+231T>C