Canonical Allele Identifier: CA2574865438
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64747023del , CM000673.2:g.64747023del GRCh38
NC_000011.9:g.64514495del , CM000673.1:g.64514495del GRCh37
NC_000011.8:g.64271071del NCBI36
NG_007574.1:g.3434del , LRG_100:g.3434del
NG_013018.1:g.18693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2313-36del MANE Select ENSP00000164139.3:n.2313-36del
ENST00000164139.3:c.2313-36del ENSP00000164139.3:n.2313-36del
ENST00000377432.7:c.2049-36del ENSP00000366650.3:n.2049-36del
ENST00000483742.1:n.1666-36del
NM_001164716.1:c.2049-36del NP_001158188.1:n.2049-36del
NM_005609.2:c.2313-36del NP_005600.1:n.2313-36del
NM_005609.3:c.2313-36del NP_005600.1:n.2313-36del
NM_005609.4:c.2313-36del MANE Select NP_005600.1:n.2313-36del