Canonical Allele Identifier: CA389699442

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51410967T>G (hg19) ; chr14:g.50944249T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944249T>G , CM000676.2:g.50944249T>G	GRCh38
NC_000014.8:g.51410967T>G , CM000676.1:g.51410967T>G	GRCh37
NC_000014.7:g.50480717T>G	NCBI36
NG_012796.1:g.5282A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.155A>C MANE Select	ENSP00000216392.7:p.Tyr52Ser
ENST00000216392.7:c.155A>C	ENSP00000216392.7:p.Tyr52Ser
ENST00000530336.2:n.222A>C
ENST00000532462.5:c.155A>C	ENSP00000431657.1:p.Tyr52Ser
ENST00000544180.6:c.155A>C	ENSP00000443787.1:p.Tyr52Ser
NM_001163940.1:c.155A>C	NP_001157412.1:p.Tyr52Ser
NM_002863.4:c.155A>C	NP_002854.3:p.Tyr52Ser
NM_002863.5:c.155A>C MANE Select	NP_002854.3:p.Tyr52Ser
NM_001163940.2:c.155A>C	NP_001157412.1:p.Tyr52Ser