Canonical Allele Identifier: CA1143447009
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508931C= , CM000663.2:g.45508931C= GRCh38
NC_000001.10:g.45974603C= , CM000663.1:g.45974603C= GRCh37
NC_000001.9:g.45747190C= NCBI36
NG_013378.1:g.13748C=

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.565C= MANE Select ENSP00000383840.4:p.Arg189=
ENST00000401061.8:c.565C= ENSP00000383840.4:p.Arg189=
ENST00000616135.1:c.394C= ENSP00000478859.1:p.Arg132=
NM_015506.2:c.565C= NP_056321.2:p.Arg189=
XM_005270724.3:c.370C= XP_005270781.1:p.Arg124=
XM_011541204.1:c.394C= XP_011539506.1:p.Arg132=
NM_001330540.1:c.394C= NP_001317469.1:p.Arg132=
XM_005270724.5:c.370C= XP_005270781.1:p.Arg124=
NM_015506.3:c.565C= MANE Select NP_056321.2:p.Arg189=
NM_001330540.2:c.394C= NP_001317469.1:p.Arg132=