Canonical Allele Identifier: CA1978919827
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64747523T= , CM000673.2:g.64747523T= GRCh38
NC_000011.9:g.64514995T= , CM000673.1:g.64514995T= GRCh37
NC_000011.8:g.64271571T= NCBI36
NG_007574.1:g.2934A= , LRG_100:g.2934A=
NG_013018.1:g.18193A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2178-165A= MANE Select ENSP00000164139.3:n.2178-165A=
ENST00000164139.3:c.2178-165A= ENSP00000164139.3:n.2178-165A=
ENST00000377432.7:c.1914-165A= ENSP00000366650.3:n.1914-165A=
ENST00000483742.1:n.1366A=
NM_001164716.1:c.1914-165A= NP_001158188.1:n.1914-165A=
NM_005609.2:c.2178-165A= NP_005600.1:n.2178-165A=
NM_005609.3:c.2178-165A= NP_005600.1:n.2178-165A=
NM_005609.4:c.2178-165A= MANE Select NP_005600.1:n.2178-165A=
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