Canonical Allele Identifier: CA2136415158
Gene: PYGL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50910207C= , CM000676.2:g.50910207C= GRCh38
NC_000014.8:g.51376925C= , CM000676.1:g.51376925C= GRCh37
NC_000014.7:g.50446675C= NCBI36
NG_012796.1:g.39324G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1970-105G= MANE Select ENSP00000216392.7:n.1970-105G=
ENST00000216392.7:c.1970-105G= ENSP00000216392.7:n.1970-105G=
ENST00000532107.2:n.143-105G=
ENST00000532462.5:c.1970-105G= ENSP00000431657.1:n.1970-105G=
ENST00000544180.6:c.1868-105G= ENSP00000443787.1:n.1868-105G=
NM_001163940.1:c.1868-105G= NP_001157412.1:n.1868-105G=
NM_002863.4:c.1970-105G= NP_002854.3:n.1970-105G=
NM_002863.5:c.1970-105G= MANE Select NP_002854.3:n.1970-105G=
NM_001163940.2:c.1868-105G= NP_001157412.1:n.1868-105G=
Search 100 bp 5'
Search 100 bp 3'