Canonical Allele Identifier: CA1143556510
Gene: MTHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11790298G= , CM000663.2:g.11790298G= GRCh38
NC_000001.10:g.11850355G= , CM000663.1:g.11850355G= GRCh37
NC_000001.9:g.11772942G= NCBI36
NG_013351.1:g.20806C= , LRG_726:g.20806C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376585.6:c.*382C= ENSP00000365770.1:n.*382C=
ENST00000376590.9:c.*382C= MANE Select ENSP00000365775.3:n.*382C=
ENST00000376592.6:c.*382C= ENSP00000365777.1:n.*382C=
ENST00000423400.7:c.*382C= ENSP00000398908.3:n.*382C=
ENST00000641446.1:c.*812C= ENSP00000493262.1:n.*812C=
ENST00000641747.1:c.*1865C= ENSP00000493116.1:n.*1865C=
ENST00000641805.1:n.2688C=
ENST00000376583.7:c.2476C= ENSP00000365767.3:n.2476C=
ENST00000376585.5:c.*382C= ENSP00000365770.1:n.*382C=
ENST00000376590.7:c.*382C= ENSP00000365775.3:n.*382C=
ENST00000376592.5:c.*382C= ENSP00000365777.1:n.*382C=
NM_005957.4:c.*382C= , LRG_726t1:c.*382C= NP_005948.3:n.*382C=
XM_005263458.2:c.*382C= XP_005263515.1:n.*382C=
XM_005263460.3:c.*382C= XP_005263517.1:n.*382C=
XM_005263461.3:c.*382C= XP_005263518.1:n.*382C=
XM_005263462.3:c.*382C= XP_005263519.1:n.*382C=
XM_005263463.2:c.*382C= XP_005263520.1:n.*382C=
XM_011541495.1:c.*382C= XP_011539797.1:n.*382C=
XM_011541496.1:c.*242C= XP_011539798.1:n.*242C=
NM_001330358.1:c.*382C= NP_001317287.1:n.*382C=
XM_005263460.5:c.*382C= XP_005263517.1:n.*382C=
XM_005263462.4:c.*382C= XP_005263519.1:n.*382C=
XM_005263463.4:c.*382C= XP_005263520.1:n.*382C=
XM_011541495.3:c.*382C= XP_011539797.1:n.*382C=
XM_011541496.3:c.*242C= XP_011539798.1:n.*242C=
XM_024447198.1:c.*382C= XP_024302966.1:n.*382C=
NM_005957.5:c.*382C= MANE Select NP_005948.3:n.*382C=
NM_001330358.2:c.*382C= NP_001317287.1:n.*382C=