Canonical Allele Identifier: CA2136419351
Gene: PYGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915876C= , CM000676.2:g.50915876C= GRCh38
NC_000014.8:g.51382594C= , CM000676.1:g.51382594C= GRCh37
NC_000014.7:g.50452344C= NCBI36
NG_012796.1:g.33655G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216392.8:c.1188G= MANE Select ENSP00000216392.7:p.Leu396=
ENST00000216392.7:c.1188G= ENSP00000216392.7:p.Leu396=
ENST00000528757.2:n.65G=
ENST00000532462.5:c.1188G= ENSP00000431657.1:p.Leu396=
ENST00000544180.6:c.1086G= ENSP00000443787.1:p.Leu362=
NM_001163940.1:c.1086G= NP_001157412.1:p.Leu362=
NM_002863.4:c.1188G= NP_002854.3:p.Leu396=
NM_002863.5:c.1188G= MANE Select NP_002854.3:p.Leu396=
NM_001163940.2:c.1086G= NP_001157412.1:p.Leu362=