Canonical Allele Identifier: CA2473783565
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1643673546

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508631del , CM000663.2:g.45508631del GRCh38
NC_000001.10:g.45974303del , CM000663.1:g.45974303del GRCh37
NC_000001.9:g.45746890del NCBI36
NG_013378.1:g.13448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.430-165del MANE Select ENSP00000383840.4:n.430-165del
ENST00000401061.8:c.430-165del ENSP00000383840.4:n.430-165del
ENST00000616135.1:c.259-165del ENSP00000478859.1:n.259-165del
NM_015506.2:c.430-165del NP_056321.2:n.430-165del
XM_005270724.3:c.235-165del XP_005270781.1:n.235-165del
XM_011541204.1:c.259-165del XP_011539506.1:n.259-165del
NM_001330540.1:c.259-165del NP_001317469.1:n.259-165del
XM_005270724.5:c.235-165del XP_005270781.1:n.235-165del
NM_015506.3:c.430-165del MANE Select NP_056321.2:n.430-165del
NM_001330540.2:c.259-165del NP_001317469.1:n.259-165del