Canonical Allele Identifier: CA1978930137
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759935G= , CM000673.2:g.64759935G= GRCh38
NC_000011.9:g.64527407G= , CM000673.1:g.64527407G= GRCh37
NC_000011.8:g.64283983G= NCBI36
NG_013018.1:g.5781C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-37C= MANE Select ENSP00000164139.3:n.-37C=
ENST00000164139.3:c.-37C= ENSP00000164139.3:n.-37C=
ENST00000377432.7:c.-37C= ENSP00000366650.3:n.-37C=
NM_001164716.1:c.-37C= NP_001158188.1:n.-37C=
NM_005609.2:c.-37C= NP_005600.1:n.-37C=
NM_005609.3:c.-37C= NP_005600.1:n.-37C=
NM_005609.4:c.-37C= MANE Select NP_005600.1:n.-37C=
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