Canonical Allele Identifier: CA1153805663
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11801257G= , CM000663.2:g.11801257G= GRCh38
NC_000001.10:g.11861314G= , CM000663.1:g.11861314G= GRCh37
NC_000001.9:g.11783901G= NCBI36
NG_008766.1:g.108G=
NG_013351.1:g.9847C= , LRG_726:g.9847C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.379C= ENSP00000365669.3:p.His127=
ENST00000376585.6:c.502C= ENSP00000365770.1:p.His168=
ENST00000376590.9:c.379C= MANE Select ENSP00000365775.3:p.His127=
ENST00000376592.6:c.379C= ENSP00000365777.1:p.His127=
ENST00000423400.7:c.499C= ENSP00000398908.3:p.His167=
ENST00000641407.1:c.379C= ENSP00000493098.1:p.His127=
ENST00000641437.1:n.511C=
ENST00000641446.1:c.379C= ENSP00000493262.1:p.His127=
ENST00000641721.1:n.436C=
ENST00000641747.1:c.237-935C= ENSP00000493116.1:n.237-935C=
ENST00000641759.1:n.514C=
ENST00000641805.1:n.662C=
ENST00000641909.1:n.789C=
ENST00000376583.7:c.502C= ENSP00000365767.3:p.His168=
ENST00000376585.5:c.502C= ENSP00000365770.1:p.His168=
ENST00000376590.7:c.379C= ENSP00000365775.3:p.His127=
ENST00000376592.5:c.379C= ENSP00000365777.1:p.His127=
ENST00000418034.1:c.379C= ENSP00000405082.1:p.His127=
NM_005957.4:c.379C= , LRG_726t1:c.379C= NP_005948.3:p.His127=
XM_005263458.2:c.502C= XP_005263515.1:p.His168=
XM_005263460.3:c.379C= XP_005263517.1:p.His127=
XM_005263461.3:c.379C= XP_005263518.1:p.His127=
XM_005263462.3:c.379C= XP_005263519.1:p.His127=
XM_005263463.2:c.133C= XP_005263520.1:p.His45=
XM_011541495.1:c.499C= XP_011539797.1:p.His167=
XM_011541496.1:c.502C= XP_011539798.1:p.His168=
NM_001330358.1:c.502C= NP_001317287.1:p.His168=
XM_005263460.5:c.379C= XP_005263517.1:p.His127=
XM_005263462.4:c.379C= XP_005263519.1:p.His127=
XM_005263463.4:c.133C= XP_005263520.1:p.His45=
XM_011541495.3:c.499C= XP_011539797.1:p.His167=
XM_011541496.3:c.502C= XP_011539798.1:p.His168=
XM_017001328.2:c.502C= XP_016856817.1:p.His168=
XM_024447198.1:c.133C= XP_024302966.1:p.His45=
XR_002956640.1:n.1246C=
NM_005957.5:c.379C= MANE Select NP_005948.3:p.His127=
NM_001330358.2:c.502C= NP_001317287.1:p.His168=