Canonical Allele Identifier: CA338478109

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11854468A>C (hg19) ; chr1:g.11794411A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794411A>C , CM000663.2:g.11794411A>C	GRCh38
NC_000001.10:g.11854468A>C , CM000663.1:g.11854468A>C	GRCh37
NC_000001.9:g.11777055A>C	NCBI36
NG_013351.1:g.16693T>G , LRG_726:g.16693T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1417T>G	ENSP00000365770.1:p.Phe473Val
ENST00000376590.9:c.1294T>G MANE Select	ENSP00000365775.3:p.Phe432Val
ENST00000376592.6:c.1294T>G	ENSP00000365777.1:p.Phe432Val
ENST00000423400.7:c.1414T>G	ENSP00000398908.3:p.Phe472Val
ENST00000641407.1:c.1294T>G	ENSP00000493098.1:p.Phe432Val
ENST00000641446.1:c.1294T>G	ENSP00000493262.1:p.Phe432Val
ENST00000641747.1:c.*806T>G	ENSP00000493116.1:n.*806T>G
ENST00000641759.1:n.1663T>G
ENST00000641805.1:n.1811T>G
ENST00000641820.1:c.559T>G	ENSP00000492937.1:p.Phe187Val
ENST00000376583.7:c.1417T>G	ENSP00000365767.3:p.Phe473Val
ENST00000376585.5:c.1417T>G	ENSP00000365770.1:p.Phe473Val
ENST00000376590.7:c.1294T>G	ENSP00000365775.3:p.Phe432Val
ENST00000376592.5:c.1294T>G	ENSP00000365777.1:p.Phe432Val
NM_005957.4:c.1294T>G , LRG_726t1:c.1294T>G	NP_005948.3:p.Phe432Val
XM_005263458.2:c.1417T>G	XP_005263515.1:p.Phe473Val
XM_005263460.3:c.1294T>G	XP_005263517.1:p.Phe432Val
XM_005263461.3:c.1294T>G	XP_005263518.1:p.Phe432Val
XM_005263462.3:c.1294T>G	XP_005263519.1:p.Phe432Val
XM_005263463.2:c.1048T>G	XP_005263520.1:p.Phe350Val
XM_011541495.1:c.1414T>G	XP_011539797.1:p.Phe472Val
XM_011541496.1:c.1417T>G	XP_011539798.1:p.Phe473Val
NM_001330358.1:c.1417T>G	NP_001317287.1:p.Phe473Val
XM_005263460.5:c.1294T>G	XP_005263517.1:p.Phe432Val
XM_005263462.4:c.1294T>G	XP_005263519.1:p.Phe432Val
XM_005263463.4:c.1048T>G	XP_005263520.1:p.Phe350Val
XM_011541495.3:c.1414T>G	XP_011539797.1:p.Phe472Val
XM_011541496.3:c.1417T>G	XP_011539798.1:p.Phe473Val
XM_017001328.2:c.1417T>G	XP_016856817.1:p.Phe473Val
XM_024447198.1:c.1048T>G	XP_024302966.1:p.Phe350Val
XR_002956640.1:n.2395T>G
NM_005957.5:c.1294T>G MANE Select	NP_005948.3:p.Phe432Val
NM_001330358.2:c.1417T>G	NP_001317287.1:p.Phe473Val