Canonical Allele Identifier: CA2643299719

Gene: MTHFR

Linked Data

• gnomAD v4: 1-11790407-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790407C>T , CM000663.2:g.11790407C>T	GRCh38
NC_000001.10:g.11850464C>T , CM000663.1:g.11850464C>T	GRCh37
NC_000001.9:g.11773051C>T	NCBI36
NG_013351.1:g.20697G>A , LRG_726:g.20697G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.*273G>A	ENSP00000365770.1:n.*273G>A
ENST00000376590.9:c.*273G>A MANE Select	ENSP00000365775.3:n.*273G>A
ENST00000376592.6:c.*273G>A	ENSP00000365777.1:n.*273G>A
ENST00000423400.7:c.*273G>A	ENSP00000398908.3:n.*273G>A
ENST00000641407.1:c.*133G>A	ENSP00000493098.1:n.*133G>A
ENST00000641446.1:c.*703G>A	ENSP00000493262.1:n.*703G>A
ENST00000641747.1:c.*1756G>A	ENSP00000493116.1:n.*1756G>A
ENST00000641805.1:n.2579G>A
ENST00000376583.7:c.2367G>A	ENSP00000365767.3:n.2367G>A
ENST00000376585.5:c.*273G>A	ENSP00000365770.1:n.*273G>A
ENST00000376590.7:c.*273G>A	ENSP00000365775.3:n.*273G>A
ENST00000376592.5:c.*273G>A	ENSP00000365777.1:n.*273G>A
NM_005957.4:c.*273G>A , LRG_726t1:c.*273G>A	NP_005948.3:n.*273G>A
XM_005263458.2:c.*273G>A	XP_005263515.1:n.*273G>A
XM_005263460.3:c.*273G>A	XP_005263517.1:n.*273G>A
XM_005263461.3:c.*273G>A	XP_005263518.1:n.*273G>A
XM_005263462.3:c.*273G>A	XP_005263519.1:n.*273G>A
XM_005263463.2:c.*273G>A	XP_005263520.1:n.*273G>A
XM_011541495.1:c.*273G>A	XP_011539797.1:n.*273G>A
XM_011541496.1:c.*133G>A	XP_011539798.1:n.*133G>A
NM_001330358.1:c.*273G>A	NP_001317287.1:n.*273G>A
XM_005263460.5:c.*273G>A	XP_005263517.1:n.*273G>A
XM_005263462.4:c.*273G>A	XP_005263519.1:n.*273G>A
XM_005263463.4:c.*273G>A	XP_005263520.1:n.*273G>A
XM_011541495.3:c.*273G>A	XP_011539797.1:n.*273G>A
XM_011541496.3:c.*133G>A	XP_011539798.1:n.*133G>A
XM_024447198.1:c.*273G>A	XP_024302966.1:n.*273G>A
NM_005957.5:c.*273G>A MANE Select	NP_005948.3:n.*273G>A
NM_001330358.2:c.*273G>A	NP_001317287.1:n.*273G>A