Canonical Allele Identifier: CA2645391254
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508262del , CM000663.2:g.45508262del GRCh38
NC_000001.10:g.45973934del , CM000663.1:g.45973934del GRCh37
NC_000001.9:g.45746521del NCBI36
NG_013378.1:g.13079del

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.327del MANE Select ENSP00000383840.4:p.Asn110ThrfsTer14
ENST00000401061.8:c.327del ENSP00000383840.4:p.Asn110ThrfsTer14
ENST00000616135.1:c.156del ENSP00000478859.1:p.Asn53ThrfsTer14
NM_015506.2:c.327del NP_056321.2:p.Asn110ThrfsTer14
XM_005270724.3:c.132del XP_005270781.1:p.Asn45ThrfsTer14
XM_011541204.1:c.156del XP_011539506.1:p.Asn53ThrfsTer14
NM_001330540.1:c.156del NP_001317469.1:p.Asn53ThrfsTer14
XM_005270724.5:c.132del XP_005270781.1:p.Asn45ThrfsTer14
NM_015506.3:c.327del MANE Select NP_056321.2:p.Asn110ThrfsTer14
NM_001330540.2:c.156del NP_001317469.1:p.Asn53ThrfsTer14