Canonical Allele Identifier: CA389682672
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50910073T>C , CM000676.2:g.50910073T>C GRCh38
NC_000014.8:g.51376791T>C , CM000676.1:g.51376791T>C GRCh37
NC_000014.7:g.50446541T>C NCBI36
NG_012796.1:g.39458A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1999A>G MANE Select ENSP00000216392.7:p.Ile667Val
ENST00000216392.7:c.1999A>G ENSP00000216392.7:p.Ile667Val
ENST00000532107.2:n.172A>G
ENST00000532462.5:c.1999A>G ENSP00000431657.1:p.Ile667Val
ENST00000544180.6:c.1897A>G ENSP00000443787.1:p.Ile633Val
NM_001163940.1:c.1897A>G NP_001157412.1:p.Ile633Val
NM_002863.4:c.1999A>G NP_002854.3:p.Ile667Val
NM_002863.5:c.1999A>G MANE Select NP_002854.3:p.Ile667Val
NM_001163940.2:c.1897A>G NP_001157412.1:p.Ile633Val