Canonical Allele Identifier: CA338480953
Gene: MTHFR HGNC NCBI

Linked Data

dbSNP Id: rs2100540460

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11796351T>A , CM000663.2:g.11796351T>A GRCh38
NC_000001.10:g.11856408T>A , CM000663.1:g.11856408T>A GRCh37
NC_000001.9:g.11778995T>A NCBI36
NG_013351.1:g.14753A>T , LRG_726:g.14753A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.635A>T ENSP00000365669.3:p.Lys212Met
ENST00000376585.6:c.758A>T ENSP00000365770.1:p.Lys253Met
ENST00000376590.9:c.635A>T MANE Select ENSP00000365775.3:p.Lys212Met
ENST00000376592.6:c.635A>T ENSP00000365777.1:p.Lys212Met
ENST00000423400.7:c.755A>T ENSP00000398908.3:p.Lys252Met
ENST00000641407.1:c.635A>T ENSP00000493098.1:p.Lys212Met
ENST00000641446.1:c.635A>T ENSP00000493262.1:p.Lys212Met
ENST00000641721.1:n.644-1003A>T
ENST00000641747.1:c.*147A>T ENSP00000493116.1:n.*147A>T
ENST00000641759.1:n.770A>T
ENST00000641805.1:n.918A>T
ENST00000641820.1:c.-101A>T ENSP00000492937.1:n.-101A>T
ENST00000376583.7:c.758A>T ENSP00000365767.3:p.Lys253Met
ENST00000376585.5:c.758A>T ENSP00000365770.1:p.Lys253Met
ENST00000376590.7:c.635A>T ENSP00000365775.3:p.Lys212Met
ENST00000376592.5:c.635A>T ENSP00000365777.1:p.Lys212Met
NM_005957.4:c.635A>T , LRG_726t1:c.635A>T NP_005948.3:p.Lys212Met
XM_005263458.2:c.758A>T XP_005263515.1:p.Lys253Met
XM_005263460.3:c.635A>T XP_005263517.1:p.Lys212Met
XM_005263461.3:c.635A>T XP_005263518.1:p.Lys212Met
XM_005263462.3:c.635A>T XP_005263519.1:p.Lys212Met
XM_005263463.2:c.389A>T XP_005263520.1:p.Lys130Met
XM_011541495.1:c.755A>T XP_011539797.1:p.Lys252Met
XM_011541496.1:c.758A>T XP_011539798.1:p.Lys253Met
NM_001330358.1:c.758A>T NP_001317287.1:p.Lys253Met
XM_005263460.5:c.635A>T XP_005263517.1:p.Lys212Met
XM_005263462.4:c.635A>T XP_005263519.1:p.Lys212Met
XM_005263463.4:c.389A>T XP_005263520.1:p.Lys130Met
XM_011541495.3:c.755A>T XP_011539797.1:p.Lys252Met
XM_011541496.3:c.758A>T XP_011539798.1:p.Lys253Met
XM_017001328.2:c.758A>T XP_016856817.1:p.Lys253Met
XM_024447198.1:c.389A>T XP_024302966.1:p.Lys130Met
XR_002956640.1:n.1502A>T
NM_005957.5:c.635A>T MANE Select NP_005948.3:p.Lys212Met
NM_001330358.2:c.758A>T NP_001317287.1:p.Lys253Met