Canonical Allele Identifier: CA1978930138
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759936A= , CM000673.2:g.64759936A= GRCh38
NC_000011.9:g.64527408A= , CM000673.1:g.64527408A= GRCh37
NC_000011.8:g.64283984A= NCBI36
NG_013018.1:g.5780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-38T= MANE Select ENSP00000164139.3:n.-38T=
ENST00000164139.3:c.-38T= ENSP00000164139.3:n.-38T=
ENST00000377432.7:c.-38T= ENSP00000366650.3:n.-38T=
NM_001164716.1:c.-38T= NP_001158188.1:n.-38T=
NM_005609.2:c.-38T= NP_005600.1:n.-38T=
NM_005609.3:c.-38T= NP_005600.1:n.-38T=
NM_005609.4:c.-38T= MANE Select NP_005600.1:n.-38T=
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