Canonical Allele Identifier: CA1978916467
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751508C= , CM000673.2:g.64751508C= GRCh38
NC_000011.9:g.64518980C= , CM000673.1:g.64518980C= GRCh37
NC_000011.8:g.64275556C= NCBI36
NG_013018.1:g.14208G=

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.1828-42G= MANE Select ENSP00000164139.3:n.1828-42G=
ENST00000164139.3:c.1828-42G= ENSP00000164139.3:n.1828-42G=
ENST00000377432.7:c.1564-42G= ENSP00000366650.3:n.1564-42G=
ENST00000462303.1:n.152-42G=
NM_001164716.1:c.1564-42G= NP_001158188.1:n.1564-42G=
NM_005609.2:c.1828-42G= NP_005600.1:n.1828-42G=
NM_005609.3:c.1828-42G= NP_005600.1:n.1828-42G=
NM_005609.4:c.1828-42G= MANE Select NP_005600.1:n.1828-42G=