Canonical Allele Identifier: CA338422897

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11862942A>T (hg19) ; chr1:g.11802885A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11802885A>T , CM000663.2:g.11802885A>T	GRCh38
NC_000001.10:g.11862942A>T , CM000663.1:g.11862942A>T	GRCh37
NC_000001.9:g.11785529A>T	NCBI36
NG_008766.1:g.1736A>T
NG_013351.1:g.8219T>A , LRG_726:g.8219T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.232T>A	ENSP00000365669.3:p.Ser78Thr
ENST00000376585.6:c.355T>A	ENSP00000365770.1:p.Ser119Thr
ENST00000376590.9:c.232T>A MANE Select	ENSP00000365775.3:p.Ser78Thr
ENST00000376592.6:c.232T>A	ENSP00000365777.1:p.Ser78Thr
ENST00000423400.7:c.352T>A	ENSP00000398908.3:p.Ser118Thr
ENST00000431243.6:n.1013T>A
ENST00000641407.1:c.232T>A	ENSP00000493098.1:p.Ser78Thr
ENST00000641437.1:n.364T>A
ENST00000641446.1:c.232T>A	ENSP00000493262.1:p.Ser78Thr
ENST00000641721.1:n.289T>A
ENST00000641747.1:c.232T>A	ENSP00000493116.1:p.Ser78Thr
ENST00000641759.1:n.367T>A
ENST00000641805.1:n.515T>A
ENST00000641909.1:n.642T>A
ENST00000642002.1:n.461T>A
ENST00000376583.7:c.355T>A	ENSP00000365767.3:p.Ser119Thr
ENST00000376585.5:c.355T>A	ENSP00000365770.1:p.Ser119Thr
ENST00000376590.7:c.232T>A	ENSP00000365775.3:p.Ser78Thr
ENST00000376592.5:c.232T>A	ENSP00000365777.1:p.Ser78Thr
ENST00000418034.1:c.232T>A	ENSP00000405082.1:p.Ser78Thr
NM_005957.4:c.232T>A , LRG_726t1:c.232T>A	NP_005948.3:p.Ser78Thr
XM_005263458.2:c.355T>A	XP_005263515.1:p.Ser119Thr
XM_005263460.3:c.232T>A	XP_005263517.1:p.Ser78Thr
XM_005263461.3:c.232T>A	XP_005263518.1:p.Ser78Thr
XM_005263462.3:c.232T>A	XP_005263519.1:p.Ser78Thr
XM_005263463.2:c.-32T>A	XP_005263520.1:n.-32T>A
XM_011541495.1:c.352T>A	XP_011539797.1:p.Ser118Thr
XM_011541496.1:c.355T>A	XP_011539798.1:p.Ser119Thr
NM_001330358.1:c.355T>A	NP_001317287.1:p.Ser119Thr
XM_005263460.5:c.232T>A	XP_005263517.1:p.Ser78Thr
XM_005263462.4:c.232T>A	XP_005263519.1:p.Ser78Thr
XM_005263463.4:c.-32T>A	XP_005263520.1:n.-32T>A
XM_011541495.3:c.352T>A	XP_011539797.1:p.Ser118Thr
XM_011541496.3:c.355T>A	XP_011539798.1:p.Ser119Thr
XM_017001328.2:c.355T>A	XP_016856817.1:p.Ser119Thr
XM_024447198.1:c.-32T>A	XP_024302966.1:n.-32T>A
XR_002956640.1:n.1099T>A
NM_005957.5:c.232T>A MANE Select	NP_005948.3:p.Ser78Thr
NM_001330358.2:c.355T>A	NP_001317287.1:p.Ser119Thr