Canonical Allele Identifier: CA2473783411
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508355G= , CM000663.2:g.45508355G= GRCh38
NC_000001.10:g.45974027G= , CM000663.1:g.45974027G= GRCh37
NC_000001.9:g.45746614G= NCBI36
NG_013378.1:g.13172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.420G= MANE Select ENSP00000383840.4:p.Trp140=
ENST00000401061.8:c.420G= ENSP00000383840.4:p.Trp140=
ENST00000616135.1:c.249G= ENSP00000478859.1:p.Trp83=
NM_015506.2:c.420G= NP_056321.2:p.Trp140=
XM_005270724.3:c.225G= XP_005270781.1:p.Trp75=
XM_011541204.1:c.249G= XP_011539506.1:p.Trp83=
NM_001330540.1:c.249G= NP_001317469.1:p.Trp83=
XM_005270724.5:c.225G= XP_005270781.1:p.Trp75=
NM_015506.3:c.420G= MANE Select NP_056321.2:p.Trp140=
NM_001330540.2:c.249G= NP_001317469.1:p.Trp83=