Canonical Allele Identifier: CA2574865123
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759930_64759931insTAG , CM000673.2:g.64759930_64759931insTAG GRCh38
NC_000011.9:g.64527402_64527403insTAG , CM000673.1:g.64527402_64527403insTAG GRCh37
NC_000011.8:g.64283978_64283979insTAG NCBI36
NG_013018.1:g.5785_5786insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-33_-32insCTA MANE Select ENSP00000164139.3:n.-33_-32insCTA
ENST00000164139.3:c.-33_-32insCTA ENSP00000164139.3:n.-33_-32insCTA
ENST00000377432.7:c.-33_-32insCTA ENSP00000366650.3:n.-33_-32insCTA
NM_001164716.1:c.-33_-32insCTA NP_001158188.1:n.-33_-32insCTA
NM_005609.2:c.-33_-32insCTA NP_005600.1:n.-33_-32insCTA
NM_005609.3:c.-33_-32insCTA NP_005600.1:n.-33_-32insCTA
NM_005609.4:c.-33_-32insCTA MANE Select NP_005600.1:n.-33_-32insCTA