Canonical Allele Identifier: CA1978930181
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759958G= , CM000673.2:g.64759958G= GRCh38
NC_000011.9:g.64527430G= , CM000673.1:g.64527430G= GRCh37
NC_000011.8:g.64284006G= NCBI36
NG_013018.1:g.5758C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-60C= MANE Select ENSP00000164139.3:n.-60C=
ENST00000164139.3:c.-60C= ENSP00000164139.3:n.-60C=
ENST00000377432.7:c.-60C= ENSP00000366650.3:n.-60C=
NM_001164716.1:c.-60C= NP_001158188.1:n.-60C=
NM_005609.2:c.-60C= NP_005600.1:n.-60C=
NM_005609.3:c.-60C= NP_005600.1:n.-60C=
NM_005609.4:c.-60C= MANE Select NP_005600.1:n.-60C=