Canonical Allele Identifier: CA2473783024
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507392C= , CM000663.2:g.45507392C= GRCh38
NC_000001.10:g.45973064C= , CM000663.1:g.45973064C= GRCh37
NC_000001.9:g.45745651C= NCBI36
NG_013378.1:g.12209C=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.118C= MANE Select ENSP00000383840.4:p.His40=
ENST00000401061.8:c.118C= ENSP00000383840.4:p.His40=
ENST00000616135.1:c.-54C= ENSP00000478859.1:n.-54C=
NM_015506.2:c.118C= NP_056321.2:p.His40=
XM_005270724.3:c.82-820C= XP_005270781.1:n.82-820C=
XM_011541204.1:c.-54C= XP_011539506.1:n.-54C=
NM_001330540.1:c.-54C= NP_001317469.1:n.-54C=
XM_005270724.5:c.82-820C= XP_005270781.1:n.82-820C=
NM_015506.3:c.118C= MANE Select NP_056321.2:p.His40=
NM_001330540.2:c.-54C= NP_001317469.1:n.-54C=