Canonical Allele Identifier: CA1143461191
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507400G= , CM000663.2:g.45507400G= GRCh38
NC_000001.10:g.45973072G= , CM000663.1:g.45973072G= GRCh37
NC_000001.9:g.45745659G= NCBI36
NG_013378.1:g.12217G=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.126G= MANE Select ENSP00000383840.4:p.Pro42=
ENST00000401061.8:c.126G= ENSP00000383840.4:p.Pro42=
ENST00000616135.1:c.-46G= ENSP00000478859.1:n.-46G=
NM_015506.2:c.126G= NP_056321.2:p.Pro42=
XM_005270724.3:c.82-812G= XP_005270781.1:n.82-812G=
XM_011541204.1:c.-46G= XP_011539506.1:n.-46G=
NM_001330540.1:c.-46G= NP_001317469.1:n.-46G=
XM_005270724.5:c.82-812G= XP_005270781.1:n.82-812G=
NM_015506.3:c.126G= MANE Select NP_056321.2:p.Pro42=
NM_001330540.2:c.-46G= NP_001317469.1:n.-46G=