Canonical Allele Identifier: CA679272315

Gene: PYGM

Linked Data

• dbSNP Id: rs1476955694
• gnomAD v3: 11-64752797-GC-G
• gnomAD v4: 11-64752797-GC-G
• MyVariant Identifiers: chr11:g.64520270del (hg19) ; chr11:g.64752798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64752802del , CM000673.2:g.64752802del	GRCh38
NC_000011.9:g.64520274del , CM000673.1:g.64520274del	GRCh37
NC_000011.8:g.64276850del	NCBI36
NG_013018.1:g.12918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.1518+275del MANE Select	ENSP00000164139.3:n.1518+275del
ENST00000164139.3:c.1518+275del	ENSP00000164139.3:n.1518+275del
ENST00000377432.7:c.1254+275del	ENSP00000366650.3:n.1254+275del
NM_001164716.1:c.1254+275del	NP_001158188.1:n.1254+275del
NM_005609.2:c.1518+275del	NP_005600.1:n.1518+275del
NM_005609.3:c.1518+275del	NP_005600.1:n.1518+275del
NM_005609.4:c.1518+275del MANE Select	NP_005600.1:n.1518+275del