Canonical Allele Identifier: CA389688515
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915874A>G , CM000676.2:g.50915874A>G GRCh38
NC_000014.8:g.51382592A>G , CM000676.1:g.51382592A>G GRCh37
NC_000014.7:g.50452342A>G NCBI36
NG_012796.1:g.33657T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216392.8:c.1190T>C MANE Select ENSP00000216392.7:p.Leu397Pro
ENST00000216392.7:c.1190T>C ENSP00000216392.7:p.Leu397Pro
ENST00000528757.2:n.67T>C
ENST00000532462.5:c.1190T>C ENSP00000431657.1:p.Leu397Pro
ENST00000544180.6:c.1088T>C ENSP00000443787.1:p.Leu363Pro
NM_001163940.1:c.1088T>C NP_001157412.1:p.Leu363Pro
NM_002863.4:c.1190T>C NP_002854.3:p.Leu397Pro
NM_002863.5:c.1190T>C MANE Select NP_002854.3:p.Leu397Pro
NM_001163940.2:c.1088T>C NP_001157412.1:p.Leu363Pro