Canonical Allele Identifier: CA1978930105
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759907G= , CM000673.2:g.64759907G= GRCh38
NC_000011.9:g.64527379G= , CM000673.1:g.64527379G= GRCh37
NC_000011.8:g.64283955G= NCBI36
NG_013018.1:g.5809C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-9C= MANE Select ENSP00000164139.3:n.-9C=
ENST00000164139.3:c.-9C= ENSP00000164139.3:n.-9C=
ENST00000377432.7:c.-9C= ENSP00000366650.3:n.-9C=
NM_001164716.1:c.-9C= NP_001158188.1:n.-9C=
NM_005609.2:c.-9C= NP_005600.1:n.-9C=
NM_005609.3:c.-9C= NP_005600.1:n.-9C=
NM_005609.4:c.-9C= MANE Select NP_005600.1:n.-9C=