Canonical Allele Identifier: CA1153792099
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11791103A= , CM000663.2:g.11791103A= GRCh38
NC_000001.10:g.11851160A= , CM000663.1:g.11851160A= GRCh37
NC_000001.9:g.11773747A= NCBI36
NG_013351.1:g.20001T= , LRG_726:g.20001T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1875+104T= ENSP00000365770.1:n.1875+104T=
ENST00000376590.9:c.1752+104T= MANE Select ENSP00000365775.3:n.1752+104T=
ENST00000376592.6:c.1752+104T= ENSP00000365777.1:n.1752+104T=
ENST00000423400.7:c.1872+104T= ENSP00000398908.3:n.1872+104T=
ENST00000641407.1:c.1752+104T= ENSP00000493098.1:n.1752+104T=
ENST00000641446.1:c.*211+104T= ENSP00000493262.1:n.*211+104T=
ENST00000641747.1:c.*1264+104T= ENSP00000493116.1:n.*1264+104T=
ENST00000641759.1:n.2121+104T=
ENST00000641805.1:n.2269+104T=
ENST00000641820.1:c.1017+104T= ENSP00000492937.1:n.1017+104T=
ENST00000376583.7:c.1875+104T= ENSP00000365767.3:n.1875+104T=
ENST00000376585.5:c.1875+104T= ENSP00000365770.1:n.1875+104T=
ENST00000376590.7:c.1752+104T= ENSP00000365775.3:n.1752+104T=
ENST00000376592.5:c.1752+104T= ENSP00000365777.1:n.1752+104T=
NM_005957.4:c.1752+104T= , LRG_726t1:c.1752+104T= NP_005948.3:n.1752+104T=
XM_005263458.2:c.1875+104T= XP_005263515.1:n.1875+104T=
XM_005263460.3:c.1752+104T= XP_005263517.1:n.1752+104T=
XM_005263461.3:c.1752+104T= XP_005263518.1:n.1752+104T=
XM_005263462.3:c.1752+104T= XP_005263519.1:n.1752+104T=
XM_005263463.2:c.1506+104T= XP_005263520.1:n.1506+104T=
XM_011541495.1:c.1872+104T= XP_011539797.1:n.1872+104T=
XM_011541496.1:c.1875+104T= XP_011539798.1:n.1875+104T=
NM_001330358.1:c.1875+104T= NP_001317287.1:n.1875+104T=
XM_005263460.5:c.1752+104T= XP_005263517.1:n.1752+104T=
XM_005263462.4:c.1752+104T= XP_005263519.1:n.1752+104T=
XM_005263463.4:c.1506+104T= XP_005263520.1:n.1506+104T=
XM_011541495.3:c.1872+104T= XP_011539797.1:n.1872+104T=
XM_011541496.3:c.1875+104T= XP_011539798.1:n.1875+104T=
XM_017001328.2:c.1875+104T= XP_016856817.1:n.1875+104T=
XM_024447198.1:c.1506+104T= XP_024302966.1:n.1506+104T=
XR_002956640.1:n.2853+104T=
NM_005957.5:c.1752+104T= MANE Select NP_005948.3:n.1752+104T=
NM_001330358.2:c.1875+104T= NP_001317287.1:n.1875+104T=