Canonical Allele Identifier: CA2136419327
Gene: PYGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915802G= , CM000676.2:g.50915802G= GRCh38
NC_000014.8:g.51382520G= , CM000676.1:g.51382520G= GRCh37
NC_000014.7:g.50452270G= NCBI36
NG_012796.1:g.33729C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1239+23C= MANE Select ENSP00000216392.7:n.1239+23C=
ENST00000216392.7:c.1239+23C= ENSP00000216392.7:n.1239+23C=
ENST00000528757.2:n.116+23C=
ENST00000532462.5:c.1239+23C= ENSP00000431657.1:n.1239+23C=
ENST00000544180.6:c.1137+23C= ENSP00000443787.1:n.1137+23C=
NM_001163940.1:c.1137+23C= NP_001157412.1:n.1137+23C=
NM_002863.4:c.1239+23C= NP_002854.3:n.1239+23C=
NM_002863.5:c.1239+23C= MANE Select NP_002854.3:n.1239+23C=
NM_001163940.2:c.1137+23C= NP_001157412.1:n.1137+23C=