Canonical Allele Identifier: CA389699049

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51410877A>T (hg19) ; chr14:g.50944159A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944159A>T , CM000676.2:g.50944159A>T	GRCh38
NC_000014.8:g.51410877A>T , CM000676.1:g.51410877A>T	GRCh37
NC_000014.7:g.50480627A>T	NCBI36
NG_012796.1:g.5372T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.243+2T>A MANE Select	ENSP00000216392.7:n.243+2T>A
ENST00000216392.7:c.243+2T>A	ENSP00000216392.7:n.243+2T>A
ENST00000530336.2:n.310+2T>A
ENST00000532462.5:c.243+2T>A	ENSP00000431657.1:n.243+2T>A
ENST00000544180.6:c.243+2T>A	ENSP00000443787.1:n.243+2T>A
NM_001163940.1:c.243+2T>A	NP_001157412.1:n.243+2T>A
NM_002863.4:c.243+2T>A	NP_002854.3:n.243+2T>A
NM_002863.5:c.243+2T>A MANE Select	NP_002854.3:n.243+2T>A
NM_001163940.2:c.243+2T>A	NP_001157412.1:n.243+2T>A