Canonical Allele Identifier: CA2136416385
Gene: PYGL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50911704T= , CM000676.2:g.50911704T= GRCh38
NC_000014.8:g.51378422T= , CM000676.1:g.51378422T= GRCh37
NC_000014.7:g.50448172T= NCBI36
NG_012796.1:g.37827A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1969+26A= MANE Select ENSP00000216392.7:n.1969+26A=
ENST00000216392.7:c.1969+26A= ENSP00000216392.7:n.1969+26A=
ENST00000532107.2:n.142+26A=
ENST00000532462.5:c.1969+26A= ENSP00000431657.1:n.1969+26A=
ENST00000544180.6:c.1867+26A= ENSP00000443787.1:n.1867+26A=
NM_001163940.1:c.1867+26A= NP_001157412.1:n.1867+26A=
NM_002863.4:c.1969+26A= NP_002854.3:n.1969+26A=
NM_002863.5:c.1969+26A= MANE Select NP_002854.3:n.1969+26A=
NM_001163940.2:c.1867+26A= NP_001157412.1:n.1867+26A=
Search 100 bp 5'
Search 100 bp 3'