Canonical Allele Identifier: CA1148444789
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508261C= , CM000663.2:g.45508261C= GRCh38
NC_000001.10:g.45973933C= , CM000663.1:g.45973933C= GRCh37
NC_000001.9:g.45746520C= NCBI36
NG_013378.1:g.13078C=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.326C= MANE Select ENSP00000383840.4:p.Pro109=
ENST00000401061.8:c.326C= ENSP00000383840.4:p.Pro109=
ENST00000616135.1:c.155C= ENSP00000478859.1:p.Pro52=
NM_015506.2:c.326C= NP_056321.2:p.Pro109=
XM_005270724.3:c.131C= XP_005270781.1:p.Pro44=
XM_011541204.1:c.155C= XP_011539506.1:p.Pro52=
NM_001330540.1:c.155C= NP_001317469.1:p.Pro52=
XM_005270724.5:c.131C= XP_005270781.1:p.Pro44=
NM_015506.3:c.326C= MANE Select NP_056321.2:p.Pro109=
NM_001330540.2:c.155C= NP_001317469.1:p.Pro52=