Canonical Allele Identifier: CA1153809457
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11802924A= , CM000663.2:g.11802924A= GRCh38
NC_000001.10:g.11862981A= , CM000663.1:g.11862981A= GRCh37
NC_000001.9:g.11785568A= NCBI36
NG_008766.1:g.1775A=
NG_013351.1:g.8180T= , LRG_726:g.8180T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376486.3:c.193T= ENSP00000365669.3:p.Phe65=
ENST00000376585.6:c.316T= ENSP00000365770.1:p.Phe106=
ENST00000376590.9:c.193T= MANE Select ENSP00000365775.3:p.Phe65=
ENST00000376592.6:c.193T= ENSP00000365777.1:p.Phe65=
ENST00000423400.7:c.313T= ENSP00000398908.3:p.Phe105=
ENST00000431243.6:n.974T=
ENST00000641407.1:c.193T= ENSP00000493098.1:p.Phe65=
ENST00000641437.1:n.325T=
ENST00000641446.1:c.193T= ENSP00000493262.1:p.Phe65=
ENST00000641721.1:n.250T=
ENST00000641747.1:c.193T= ENSP00000493116.1:p.Phe65=
ENST00000641759.1:n.328T=
ENST00000641805.1:n.476T=
ENST00000641909.1:n.603T=
ENST00000642002.1:n.422T=
ENST00000376583.7:c.316T= ENSP00000365767.3:p.Phe106=
ENST00000376585.5:c.316T= ENSP00000365770.1:p.Phe106=
ENST00000376590.7:c.193T= ENSP00000365775.3:p.Phe65=
ENST00000376592.5:c.193T= ENSP00000365777.1:p.Phe65=
ENST00000418034.1:c.193T= ENSP00000405082.1:p.Phe65=
NM_005957.4:c.193T= , LRG_726t1:c.193T= NP_005948.3:p.Phe65=
XM_005263458.2:c.316T= XP_005263515.1:p.Phe106=
XM_005263460.3:c.193T= XP_005263517.1:p.Phe65=
XM_005263461.3:c.193T= XP_005263518.1:p.Phe65=
XM_005263462.3:c.193T= XP_005263519.1:p.Phe65=
XM_005263463.2:c.-71T= XP_005263520.1:n.-71T=
XM_011541495.1:c.313T= XP_011539797.1:p.Phe105=
XM_011541496.1:c.316T= XP_011539798.1:p.Phe106=
NM_001330358.1:c.316T= NP_001317287.1:p.Phe106=
XM_005263460.5:c.193T= XP_005263517.1:p.Phe65=
XM_005263462.4:c.193T= XP_005263519.1:p.Phe65=
XM_005263463.4:c.-71T= XP_005263520.1:n.-71T=
XM_011541495.3:c.313T= XP_011539797.1:p.Phe105=
XM_011541496.3:c.316T= XP_011539798.1:p.Phe106=
XM_017001328.2:c.316T= XP_016856817.1:p.Phe106=
XM_024447198.1:c.-71T= XP_024302966.1:n.-71T=
XR_002956640.1:n.1060T=
NM_005957.5:c.193T= MANE Select NP_005948.3:p.Phe65=
NM_001330358.2:c.316T= NP_001317287.1:p.Phe106=