Canonical Allele Identifier: CA1153810429
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11800053A= , CM000663.2:g.11800053A= GRCh38
NC_000001.10:g.11860110A= , CM000663.1:g.11860110A= GRCh37
NC_000001.9:g.11782697A= NCBI36
NG_013351.1:g.11051T= , LRG_726:g.11051T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.586+159T= ENSP00000365669.3:n.586+159T=
ENST00000376585.6:c.709+159T= ENSP00000365770.1:n.709+159T=
ENST00000376590.9:c.586+159T= MANE Select ENSP00000365775.3:n.586+159T=
ENST00000376592.6:c.586+159T= ENSP00000365777.1:n.586+159T=
ENST00000423400.7:c.706+159T= ENSP00000398908.3:n.706+159T=
ENST00000641407.1:c.586+159T= ENSP00000493098.1:n.586+159T=
ENST00000641437.1:n.1715T=
ENST00000641446.1:c.586+159T= ENSP00000493262.1:n.586+159T=
ENST00000641721.1:n.643+159T=
ENST00000641747.1:c.*98+159T= ENSP00000493116.1:n.*98+159T=
ENST00000641759.1:n.721+159T=
ENST00000641805.1:n.869+159T=
ENST00000641909.1:n.1993T=
ENST00000376583.7:c.709+159T= ENSP00000365767.3:n.709+159T=
ENST00000376585.5:c.709+159T= ENSP00000365770.1:n.709+159T=
ENST00000376590.7:c.586+159T= ENSP00000365775.3:n.586+159T=
ENST00000376592.5:c.586+159T= ENSP00000365777.1:n.586+159T=
NM_005957.4:c.586+159T= , LRG_726t1:c.586+159T= NP_005948.3:n.586+159T=
XM_005263458.2:c.709+159T= XP_005263515.1:n.709+159T=
XM_005263460.3:c.586+159T= XP_005263517.1:n.586+159T=
XM_005263461.3:c.586+159T= XP_005263518.1:n.586+159T=
XM_005263462.3:c.586+159T= XP_005263519.1:n.586+159T=
XM_005263463.2:c.340+159T= XP_005263520.1:n.340+159T=
XM_011541495.1:c.706+159T= XP_011539797.1:n.706+159T=
XM_011541496.1:c.709+159T= XP_011539798.1:n.709+159T=
NM_001330358.1:c.709+159T= NP_001317287.1:n.709+159T=
XM_005263460.5:c.586+159T= XP_005263517.1:n.586+159T=
XM_005263462.4:c.586+159T= XP_005263519.1:n.586+159T=
XM_005263463.4:c.340+159T= XP_005263520.1:n.340+159T=
XM_011541495.3:c.706+159T= XP_011539797.1:n.706+159T=
XM_011541496.3:c.709+159T= XP_011539798.1:n.709+159T=
XM_017001328.2:c.709+159T= XP_016856817.1:n.709+159T=
XM_024447198.1:c.340+159T= XP_024302966.1:n.340+159T=
XR_002956640.1:n.1453+159T=
NM_005957.5:c.586+159T= MANE Select NP_005948.3:n.586+159T=
NM_001330358.2:c.709+159T= NP_001317287.1:n.709+159T=