Canonical Allele Identifier: CA338480845

Gene: MTHFR

Linked Data

• MyVariant Identifiers: chr1:g.11856385C>A (hg19) ; chr1:g.11796328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796328C>A , CM000663.2:g.11796328C>A	GRCh38
NC_000001.10:g.11856385C>A , CM000663.1:g.11856385C>A	GRCh37
NC_000001.9:g.11778972C>A	NCBI36
NG_013351.1:g.14776G>T , LRG_726:g.14776G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.658G>T	ENSP00000365669.3:p.Ala220Ser
ENST00000376585.6:c.781G>T	ENSP00000365770.1:p.Ala261Ser
ENST00000376590.9:c.658G>T MANE Select	ENSP00000365775.3:p.Ala220Ser
ENST00000376592.6:c.658G>T	ENSP00000365777.1:p.Ala220Ser
ENST00000423400.7:c.778G>T	ENSP00000398908.3:p.Ala260Ser
ENST00000641407.1:c.658G>T	ENSP00000493098.1:p.Ala220Ser
ENST00000641446.1:c.658G>T	ENSP00000493262.1:p.Ala220Ser
ENST00000641721.1:n.644-980G>T
ENST00000641747.1:c.*170G>T	ENSP00000493116.1:n.*170G>T
ENST00000641759.1:n.793G>T
ENST00000641805.1:n.941G>T
ENST00000641820.1:c.-78G>T	ENSP00000492937.1:n.-78G>T
ENST00000376583.7:c.781G>T	ENSP00000365767.3:p.Ala261Ser
ENST00000376585.5:c.781G>T	ENSP00000365770.1:p.Ala261Ser
ENST00000376590.7:c.658G>T	ENSP00000365775.3:p.Ala220Ser
ENST00000376592.5:c.658G>T	ENSP00000365777.1:p.Ala220Ser
NM_005957.4:c.658G>T , LRG_726t1:c.658G>T	NP_005948.3:p.Ala220Ser
XM_005263458.2:c.781G>T	XP_005263515.1:p.Ala261Ser
XM_005263460.3:c.658G>T	XP_005263517.1:p.Ala220Ser
XM_005263461.3:c.658G>T	XP_005263518.1:p.Ala220Ser
XM_005263462.3:c.658G>T	XP_005263519.1:p.Ala220Ser
XM_005263463.2:c.412G>T	XP_005263520.1:p.Ala138Ser
XM_011541495.1:c.778G>T	XP_011539797.1:p.Ala260Ser
XM_011541496.1:c.781G>T	XP_011539798.1:p.Ala261Ser
NM_001330358.1:c.781G>T	NP_001317287.1:p.Ala261Ser
XM_005263460.5:c.658G>T	XP_005263517.1:p.Ala220Ser
XM_005263462.4:c.658G>T	XP_005263519.1:p.Ala220Ser
XM_005263463.4:c.412G>T	XP_005263520.1:p.Ala138Ser
XM_011541495.3:c.778G>T	XP_011539797.1:p.Ala260Ser
XM_011541496.3:c.781G>T	XP_011539798.1:p.Ala261Ser
XM_017001328.2:c.781G>T	XP_016856817.1:p.Ala261Ser
XM_024447198.1:c.412G>T	XP_024302966.1:p.Ala138Ser
XR_002956640.1:n.1525G>T
NM_005957.5:c.658G>T MANE Select	NP_005948.3:p.Ala220Ser
NM_001330358.2:c.781G>T	NP_001317287.1:p.Ala261Ser