Canonical Allele Identifier: CA389699521
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50944268C>G , CM000676.2:g.50944268C>G GRCh38
NC_000014.8:g.51410986C>G , CM000676.1:g.51410986C>G GRCh37
NC_000014.7:g.50480736C>G NCBI36
NG_012796.1:g.5263G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.136G>C MANE Select ENSP00000216392.7:p.Val46Leu
ENST00000216392.7:c.136G>C ENSP00000216392.7:p.Val46Leu
ENST00000530336.2:n.203G>C
ENST00000532462.5:c.136G>C ENSP00000431657.1:p.Val46Leu
ENST00000544180.6:c.136G>C ENSP00000443787.1:p.Val46Leu
NM_001163940.1:c.136G>C NP_001157412.1:p.Val46Leu
NM_002863.4:c.136G>C NP_002854.3:p.Val46Leu
NM_002863.5:c.136G>C MANE Select NP_002854.3:p.Val46Leu
NM_001163940.2:c.136G>C NP_001157412.1:p.Val46Leu