Canonical Allele Identifier: CA338480284

Gene: MTHFR

Linked Data

• dbSNP Id: rs367992906
• gnomAD v2: 1-11855295-A-T
• gnomAD v4: 1-11795238-A-T
• MyVariant Identifiers: chr1:g.11855295A>T (hg19) ; chr1:g.11795238A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11795238A>T , CM000663.2:g.11795238A>T	GRCh38
NC_000001.10:g.11855295A>T , CM000663.1:g.11855295A>T	GRCh37
NC_000001.9:g.11777882A>T	NCBI36
NG_013351.1:g.15866T>A , LRG_726:g.15866T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1014T>A	ENSP00000365770.1:p.Tyr338Ter
ENST00000376590.9:c.891T>A MANE Select	ENSP00000365775.3:p.Tyr297Ter
ENST00000376592.6:c.891T>A	ENSP00000365777.1:p.Tyr297Ter
ENST00000423400.7:c.1011T>A	ENSP00000398908.3:p.Tyr337Ter
ENST00000641407.1:c.891T>A	ENSP00000493098.1:p.Tyr297Ter
ENST00000641446.1:c.891T>A	ENSP00000493262.1:p.Tyr297Ter
ENST00000641721.1:n.754T>A
ENST00000641747.1:c.*403T>A	ENSP00000493116.1:n.*403T>A
ENST00000641759.1:n.1026T>A
ENST00000641805.1:n.1174T>A
ENST00000641820.1:c.156T>A	ENSP00000492937.1:p.Tyr52Ter
ENST00000376583.7:c.1014T>A	ENSP00000365767.3:p.Tyr338Ter
ENST00000376585.5:c.1014T>A	ENSP00000365770.1:p.Tyr338Ter
ENST00000376590.7:c.891T>A	ENSP00000365775.3:p.Tyr297Ter
ENST00000376592.5:c.891T>A	ENSP00000365777.1:p.Tyr297Ter
NM_005957.4:c.891T>A , LRG_726t1:c.891T>A	NP_005948.3:p.Tyr297Ter
XM_005263458.2:c.1014T>A	XP_005263515.1:p.Tyr338Ter
XM_005263460.3:c.891T>A	XP_005263517.1:p.Tyr297Ter
XM_005263461.3:c.891T>A	XP_005263518.1:p.Tyr297Ter
XM_005263462.3:c.891T>A	XP_005263519.1:p.Tyr297Ter
XM_005263463.2:c.645T>A	XP_005263520.1:p.Tyr215Ter
XM_011541495.1:c.1011T>A	XP_011539797.1:p.Tyr337Ter
XM_011541496.1:c.1014T>A	XP_011539798.1:p.Tyr338Ter
NM_001330358.1:c.1014T>A	NP_001317287.1:p.Tyr338Ter
XM_005263460.5:c.891T>A	XP_005263517.1:p.Tyr297Ter
XM_005263462.4:c.891T>A	XP_005263519.1:p.Tyr297Ter
XM_005263463.4:c.645T>A	XP_005263520.1:p.Tyr215Ter
XM_011541495.3:c.1011T>A	XP_011539797.1:p.Tyr337Ter
XM_011541496.3:c.1014T>A	XP_011539798.1:p.Tyr338Ter
XM_017001328.2:c.1014T>A	XP_016856817.1:p.Tyr338Ter
XM_024447198.1:c.645T>A	XP_024302966.1:p.Tyr215Ter
XR_002956640.1:n.1758T>A
NM_005957.5:c.891T>A MANE Select	NP_005948.3:p.Tyr297Ter
NM_001330358.2:c.1014T>A	NP_001317287.1:p.Tyr338Ter