Canonical Allele Identifier: CA338474583

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11851350G>T (hg19) ; chr1:g.11791293G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11791293G>T , CM000663.2:g.11791293G>T	GRCh38
NC_000001.10:g.11851350G>T , CM000663.1:g.11851350G>T	GRCh37
NC_000001.9:g.11773937G>T	NCBI36
NG_013351.1:g.19811C>A , LRG_726:g.19811C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1789C>A	ENSP00000365770.1:p.Pro597Thr
ENST00000376590.9:c.1666C>A MANE Select	ENSP00000365775.3:p.Pro556Thr
ENST00000376592.6:c.1666C>A	ENSP00000365777.1:p.Pro556Thr
ENST00000423400.7:c.1786C>A	ENSP00000398908.3:p.Pro596Thr
ENST00000641407.1:c.1666C>A	ENSP00000493098.1:p.Pro556Thr
ENST00000641446.1:c.*125C>A	ENSP00000493262.1:n.*125C>A
ENST00000641747.1:c.*1178C>A	ENSP00000493116.1:n.*1178C>A
ENST00000641759.1:n.2035C>A
ENST00000641805.1:n.2183C>A
ENST00000641820.1:c.931C>A	ENSP00000492937.1:p.Pro311Thr
ENST00000376583.7:c.1789C>A	ENSP00000365767.3:p.Pro597Thr
ENST00000376585.5:c.1789C>A	ENSP00000365770.1:p.Pro597Thr
ENST00000376590.7:c.1666C>A	ENSP00000365775.3:p.Pro556Thr
ENST00000376592.5:c.1666C>A	ENSP00000365777.1:p.Pro556Thr
NM_005957.4:c.1666C>A , LRG_726t1:c.1666C>A	NP_005948.3:p.Pro556Thr
XM_005263458.2:c.1789C>A	XP_005263515.1:p.Pro597Thr
XM_005263460.3:c.1666C>A	XP_005263517.1:p.Pro556Thr
XM_005263461.3:c.1666C>A	XP_005263518.1:p.Pro556Thr
XM_005263462.3:c.1666C>A	XP_005263519.1:p.Pro556Thr
XM_005263463.2:c.1420C>A	XP_005263520.1:p.Pro474Thr
XM_011541495.1:c.1786C>A	XP_011539797.1:p.Pro596Thr
XM_011541496.1:c.1789C>A	XP_011539798.1:p.Pro597Thr
NM_001330358.1:c.1789C>A	NP_001317287.1:p.Pro597Thr
XM_005263460.5:c.1666C>A	XP_005263517.1:p.Pro556Thr
XM_005263462.4:c.1666C>A	XP_005263519.1:p.Pro556Thr
XM_005263463.4:c.1420C>A	XP_005263520.1:p.Pro474Thr
XM_011541495.3:c.1786C>A	XP_011539797.1:p.Pro596Thr
XM_011541496.3:c.1789C>A	XP_011539798.1:p.Pro597Thr
XM_017001328.2:c.1789C>A	XP_016856817.1:p.Pro597Thr
XM_024447198.1:c.1420C>A	XP_024302966.1:p.Pro474Thr
XR_002956640.1:n.2767C>A
NM_005957.5:c.1666C>A MANE Select	NP_005948.3:p.Pro556Thr
NM_001330358.2:c.1789C>A	NP_001317287.1:p.Pro597Thr