Canonical Allele Identifier: CA1978928673
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758719G= , CM000673.2:g.64758719G= GRCh38
NC_000011.9:g.64526191G= , CM000673.1:g.64526191G= GRCh37
NC_000011.8:g.64282767G= NCBI36
NG_013018.1:g.6997C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.244-15C= MANE Select ENSP00000164139.3:n.244-15C=
ENST00000164139.3:c.244-15C= ENSP00000164139.3:n.244-15C=
ENST00000377432.7:c.244-453C= ENSP00000366650.3:n.244-453C=
NM_001164716.1:c.244-453C= NP_001158188.1:n.244-453C=
NM_005609.2:c.244-15C= NP_005600.1:n.244-15C=
NM_005609.3:c.244-15C= NP_005600.1:n.244-15C=
NM_005609.4:c.244-15C= MANE Select NP_005600.1:n.244-15C=