Canonical Allele Identifier: CA338473883

Gene: MTHFR

Linked Data

• dbSNP Id: rs1644072699
• MyVariant Identifiers: chr1:g.11850905C>G (hg19) ; chr1:g.11790848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790848C>G , CM000663.2:g.11790848C>G	GRCh38
NC_000001.10:g.11850905C>G , CM000663.1:g.11850905C>G	GRCh37
NC_000001.9:g.11773492C>G	NCBI36
NG_013351.1:g.20256G>C , LRG_726:g.20256G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1926G>C	ENSP00000365770.1:p.Glu642Asp
ENST00000376590.9:c.1803G>C MANE Select	ENSP00000365775.3:p.Glu601Asp
ENST00000376592.6:c.1803G>C	ENSP00000365777.1:p.Glu601Asp
ENST00000423400.7:c.1923G>C	ENSP00000398908.3:p.Glu641Asp
ENST00000641407.1:c.1753-132G>C	ENSP00000493098.1:n.1753-132G>C
ENST00000641446.1:c.*262G>C	ENSP00000493262.1:n.*262G>C
ENST00000641747.1:c.*1315G>C	ENSP00000493116.1:n.*1315G>C
ENST00000641759.1:n.2172G>C
ENST00000641805.1:n.2270-132G>C
ENST00000641820.1:c.1068G>C	ENSP00000492937.1:p.Glu356Asp
ENST00000376583.7:c.1926G>C	ENSP00000365767.3:p.Glu642Asp
ENST00000376585.5:c.1926G>C	ENSP00000365770.1:p.Glu642Asp
ENST00000376590.7:c.1803G>C	ENSP00000365775.3:p.Glu601Asp
ENST00000376592.5:c.1803G>C	ENSP00000365777.1:p.Glu601Asp
NM_005957.4:c.1803G>C , LRG_726t1:c.1803G>C	NP_005948.3:p.Glu601Asp
XM_005263458.2:c.1926G>C	XP_005263515.1:p.Glu642Asp
XM_005263460.3:c.1803G>C	XP_005263517.1:p.Glu601Asp
XM_005263461.3:c.1803G>C	XP_005263518.1:p.Glu601Asp
XM_005263462.3:c.1803G>C	XP_005263519.1:p.Glu601Asp
XM_005263463.2:c.1557G>C	XP_005263520.1:p.Glu519Asp
XM_011541495.1:c.1923G>C	XP_011539797.1:p.Glu641Asp
XM_011541496.1:c.1876-132G>C	XP_011539798.1:n.1876-132G>C
NM_001330358.1:c.1926G>C	NP_001317287.1:p.Glu642Asp
XM_005263460.5:c.1803G>C	XP_005263517.1:p.Glu601Asp
XM_005263462.4:c.1803G>C	XP_005263519.1:p.Glu601Asp
XM_005263463.4:c.1557G>C	XP_005263520.1:p.Glu519Asp
XM_011541495.3:c.1923G>C	XP_011539797.1:p.Glu641Asp
XM_011541496.3:c.1876-132G>C	XP_011539798.1:n.1876-132G>C
XM_017001328.2:c.1876-100G>C	XP_016856817.1:n.1876-100G>C
XM_024447198.1:c.1557G>C	XP_024302966.1:p.Glu519Asp
XR_002956640.1:n.2854-132G>C
NM_005957.5:c.1803G>C MANE Select	NP_005948.3:p.Glu601Asp
NM_001330358.2:c.1926G>C	NP_001317287.1:p.Glu642Asp