Canonical Allele Identifier: CA2614199685

Gene: PYGM

Linked Data

• gnomAD v4: 11-64747528-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747529dup , CM000673.2:g.64747529dup	GRCh38
NC_000011.9:g.64515001dup , CM000673.1:g.64515001dup	GRCh37
NC_000011.8:g.64271577dup	NCBI36
NG_007574.1:g.2928dup , LRG_100:g.2928dup
NG_013018.1:g.18187dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2178-171dup MANE Select	ENSP00000164139.3:n.2178-171dup
ENST00000164139.3:c.2178-171dup	ENSP00000164139.3:n.2178-171dup
ENST00000377432.7:c.1914-171dup	ENSP00000366650.3:n.1914-171dup
ENST00000483742.1:n.1360dup
NM_001164716.1:c.1914-171dup	NP_001158188.1:n.1914-171dup
NM_005609.2:c.2178-171dup	NP_005600.1:n.2178-171dup
NM_005609.3:c.2178-171dup	NP_005600.1:n.2178-171dup
NM_005609.4:c.2178-171dup MANE Select	NP_005600.1:n.2178-171dup