Canonical Allele Identifier: CA2586966643
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508932_45508940del , CM000663.2:g.45508932_45508940del GRCh38
NC_000001.10:g.45974604_45974612del , CM000663.1:g.45974604_45974612del GRCh37
NC_000001.9:g.45747191_45747199del NCBI36
NG_013378.1:g.13749_13757del

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.566_574del MANE Select ENSP00000383840.4:p.Arg189_Ala191del
ENST00000401061.8:c.566_574del ENSP00000383840.4:p.Arg189_Ala191del
ENST00000616135.1:c.395_403del ENSP00000478859.1:p.Arg132_Ala134del
NM_015506.2:c.566_574del NP_056321.2:p.Arg189_Ala191del
XM_005270724.3:c.371_379del XP_005270781.1:p.Arg124_Ala126del
XM_011541204.1:c.395_403del XP_011539506.1:p.Arg132_Ala134del
NM_001330540.1:c.395_403del NP_001317469.1:p.Arg132_Ala134del
XM_005270724.5:c.371_379del XP_005270781.1:p.Arg124_Ala126del
NM_015506.3:c.566_574del MANE Select NP_056321.2:p.Arg189_Ala191del
NM_001330540.2:c.395_403del NP_001317469.1:p.Arg132_Ala134del