Canonical Allele Identifier: CA389682621

Gene: PYGL

Linked Data

• gnomAD v4: 14-50910057-G-A
• MyVariant Identifiers: chr14:g.51376775G>A (hg19) ; chr14:g.50910057G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50910057G>A , CM000676.2:g.50910057G>A	GRCh38
NC_000014.8:g.51376775G>A , CM000676.1:g.51376775G>A	GRCh37
NC_000014.7:g.50446525G>A	NCBI36
NG_012796.1:g.39474C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.2015C>T MANE Select	ENSP00000216392.7:p.Thr672Ile
ENST00000216392.7:c.2015C>T	ENSP00000216392.7:p.Thr672Ile
ENST00000532107.2:n.188C>T
ENST00000532462.5:c.2015C>T	ENSP00000431657.1:p.Thr672Ile
ENST00000544180.6:c.1913C>T	ENSP00000443787.1:p.Thr638Ile
NM_001163940.1:c.1913C>T	NP_001157412.1:p.Thr638Ile
NM_002863.4:c.2015C>T	NP_002854.3:p.Thr672Ile
NM_002863.5:c.2015C>T MANE Select	NP_002854.3:p.Thr672Ile
NM_001163940.2:c.1913C>T	NP_001157412.1:p.Thr638Ile