Canonical Allele Identifier: CA1153809495
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11802945T= , CM000663.2:g.11802945T= GRCh38
NC_000001.10:g.11863002T= , CM000663.1:g.11863002T= GRCh37
NC_000001.9:g.11785589T= NCBI36
NG_008766.1:g.1796T=
NG_013351.1:g.8159A= , LRG_726:g.8159A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.172A= ENSP00000365669.3:p.Lys58=
ENST00000376585.6:c.295A= ENSP00000365770.1:p.Lys99=
ENST00000376590.9:c.172A= MANE Select ENSP00000365775.3:p.Lys58=
ENST00000376592.6:c.172A= ENSP00000365777.1:p.Lys58=
ENST00000423400.7:c.292A= ENSP00000398908.3:p.Lys98=
ENST00000431243.6:n.953A=
ENST00000641407.1:c.172A= ENSP00000493098.1:p.Lys58=
ENST00000641437.1:n.304A=
ENST00000641446.1:c.172A= ENSP00000493262.1:p.Lys58=
ENST00000641721.1:n.229A=
ENST00000641747.1:c.172A= ENSP00000493116.1:p.Lys58=
ENST00000641759.1:n.307A=
ENST00000641805.1:n.455A=
ENST00000641909.1:n.582A=
ENST00000642002.1:n.401A=
ENST00000376583.7:c.295A= ENSP00000365767.3:p.Lys99=
ENST00000376585.5:c.295A= ENSP00000365770.1:p.Lys99=
ENST00000376590.7:c.172A= ENSP00000365775.3:p.Lys58=
ENST00000376592.5:c.172A= ENSP00000365777.1:p.Lys58=
ENST00000418034.1:c.172A= ENSP00000405082.1:p.Lys58=
NM_005957.4:c.172A= , LRG_726t1:c.172A= NP_005948.3:p.Lys58=
XM_005263458.2:c.295A= XP_005263515.1:p.Lys99=
XM_005263460.3:c.172A= XP_005263517.1:p.Lys58=
XM_005263461.3:c.172A= XP_005263518.1:p.Lys58=
XM_005263462.3:c.172A= XP_005263519.1:p.Lys58=
XM_005263463.2:c.-92A= XP_005263520.1:n.-92A=
XM_011541495.1:c.292A= XP_011539797.1:p.Lys98=
XM_011541496.1:c.295A= XP_011539798.1:p.Lys99=
NM_001330358.1:c.295A= NP_001317287.1:p.Lys99=
XM_005263460.5:c.172A= XP_005263517.1:p.Lys58=
XM_005263462.4:c.172A= XP_005263519.1:p.Lys58=
XM_005263463.4:c.-92A= XP_005263520.1:n.-92A=
XM_011541495.3:c.292A= XP_011539797.1:p.Lys98=
XM_011541496.3:c.295A= XP_011539798.1:p.Lys99=
XM_017001328.2:c.295A= XP_016856817.1:p.Lys99=
XM_024447198.1:c.-92A= XP_024302966.1:n.-92A=
XR_002956640.1:n.1039A=
NM_005957.5:c.172A= MANE Select NP_005948.3:p.Lys58=
NM_001330358.2:c.295A= NP_001317287.1:p.Lys99=