Canonical Allele Identifier: CA389699136
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50944177T>G , CM000676.2:g.50944177T>G GRCh38
NC_000014.8:g.51410895T>G , CM000676.1:g.51410895T>G GRCh37
NC_000014.7:g.50480645T>G NCBI36
NG_012796.1:g.5354A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.227A>C MANE Select ENSP00000216392.7:p.Tyr76Ser
ENST00000216392.7:c.227A>C ENSP00000216392.7:p.Tyr76Ser
ENST00000530336.2:n.294A>C
ENST00000532462.5:c.227A>C ENSP00000431657.1:p.Tyr76Ser
ENST00000544180.6:c.227A>C ENSP00000443787.1:p.Tyr76Ser
NM_001163940.1:c.227A>C NP_001157412.1:p.Tyr76Ser
NM_002863.4:c.227A>C NP_002854.3:p.Tyr76Ser
NM_002863.5:c.227A>C MANE Select NP_002854.3:p.Tyr76Ser
NM_001163940.2:c.227A>C NP_001157412.1:p.Tyr76Ser