Canonical Allele Identifier: CA1153799655
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11794713G= , CM000663.2:g.11794713G= GRCh38
NC_000001.10:g.11854770G= , CM000663.1:g.11854770G= GRCh37
NC_000001.9:g.11777357G= NCBI36
NG_013351.1:g.16391C= , LRG_726:g.16391C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1289+16C= ENSP00000365770.1:n.1289+16C=
ENST00000376590.9:c.1166+16C= MANE Select ENSP00000365775.3:n.1166+16C=
ENST00000376592.6:c.1166+16C= ENSP00000365777.1:n.1166+16C=
ENST00000423400.7:c.1286+16C= ENSP00000398908.3:n.1286+16C=
ENST00000641407.1:c.1166+16C= ENSP00000493098.1:n.1166+16C=
ENST00000641446.1:c.1166+16C= ENSP00000493262.1:n.1166+16C=
ENST00000641747.1:c.*678+16C= ENSP00000493116.1:n.*678+16C=
ENST00000641759.1:n.1535+16C=
ENST00000641805.1:n.1683+16C=
ENST00000641820.1:c.431+16C= ENSP00000492937.1:n.431+16C=
ENST00000376583.7:c.1289+16C= ENSP00000365767.3:n.1289+16C=
ENST00000376585.5:c.1289+16C= ENSP00000365770.1:n.1289+16C=
ENST00000376590.7:c.1166+16C= ENSP00000365775.3:n.1166+16C=
ENST00000376592.5:c.1166+16C= ENSP00000365777.1:n.1166+16C=
NM_005957.4:c.1166+16C= , LRG_726t1:c.1166+16C= NP_005948.3:n.1166+16C=
XM_005263458.2:c.1289+16C= XP_005263515.1:n.1289+16C=
XM_005263460.3:c.1166+16C= XP_005263517.1:n.1166+16C=
XM_005263461.3:c.1166+16C= XP_005263518.1:n.1166+16C=
XM_005263462.3:c.1166+16C= XP_005263519.1:n.1166+16C=
XM_005263463.2:c.920+16C= XP_005263520.1:n.920+16C=
XM_011541495.1:c.1286+16C= XP_011539797.1:n.1286+16C=
XM_011541496.1:c.1289+16C= XP_011539798.1:n.1289+16C=
NM_001330358.1:c.1289+16C= NP_001317287.1:n.1289+16C=
XM_005263460.5:c.1166+16C= XP_005263517.1:n.1166+16C=
XM_005263462.4:c.1166+16C= XP_005263519.1:n.1166+16C=
XM_005263463.4:c.920+16C= XP_005263520.1:n.920+16C=
XM_011541495.3:c.1286+16C= XP_011539797.1:n.1286+16C=
XM_011541496.3:c.1289+16C= XP_011539798.1:n.1289+16C=
XM_017001328.2:c.1289+16C= XP_016856817.1:n.1289+16C=
XM_024447198.1:c.920+16C= XP_024302966.1:n.920+16C=
XR_002956640.1:n.2267+16C=
NM_005957.5:c.1166+16C= MANE Select NP_005948.3:n.1166+16C=
NM_001330358.2:c.1289+16C= NP_001317287.1:n.1289+16C=