Canonical Allele Identifier: CA1978919738

Gene: PYGM

Linked Data

• dbSNP Id: rs2058323257
• gnomAD v4: 11-64747472-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747476del , CM000673.2:g.64747476del	GRCh38
NC_000011.9:g.64514948del , CM000673.1:g.64514948del	GRCh37
NC_000011.8:g.64271524del	NCBI36
NG_007574.1:g.2984del , LRG_100:g.2984del
NG_013018.1:g.18243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2178-115del MANE Select	ENSP00000164139.3:n.2178-115del
ENST00000164139.3:c.2178-115del	ENSP00000164139.3:n.2178-115del
ENST00000377432.7:c.1914-115del	ENSP00000366650.3:n.1914-115del
ENST00000483742.1:n.1416del
NM_001164716.1:c.1914-115del	NP_001158188.1:n.1914-115del
NM_005609.2:c.2178-115del	NP_005600.1:n.2178-115del
NM_005609.3:c.2178-115del	NP_005600.1:n.2178-115del
NM_005609.4:c.2178-115del MANE Select	NP_005600.1:n.2178-115del