Canonical Allele Identifier: CA1978928714
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758777C= , CM000673.2:g.64758777C= GRCh38
NC_000011.9:g.64526249C= , CM000673.1:g.64526249C= GRCh37
NC_000011.8:g.64282825C= NCBI36
NG_013018.1:g.6939G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.244-73G= MANE Select ENSP00000164139.3:n.244-73G=
ENST00000164139.3:c.244-73G= ENSP00000164139.3:n.244-73G=
ENST00000377432.7:c.244-511G= ENSP00000366650.3:n.244-511G=
NM_001164716.1:c.244-511G= NP_001158188.1:n.244-511G=
NM_005609.2:c.244-73G= NP_005600.1:n.244-73G=
NM_005609.3:c.244-73G= NP_005600.1:n.244-73G=
NM_005609.4:c.244-73G= MANE Select NP_005600.1:n.244-73G=