Canonical Allele Identifier: CA1978929873
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759749T= , CM000673.2:g.64759749T= GRCh38
NC_000011.9:g.64527221T= , CM000673.1:g.64527221T= GRCh37
NC_000011.8:g.64283797T= NCBI36
NG_013018.1:g.5967A=

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.150A= MANE Select ENSP00000164139.3:p.Arg50=
ENST00000164139.3:c.150A= ENSP00000164139.3:p.Arg50=
ENST00000377432.7:c.150A= ENSP00000366650.3:p.Arg50=
NM_001164716.1:c.150A= NP_001158188.1:p.Arg50=
NM_005609.2:c.150A= NP_005600.1:p.Arg50=
NM_005609.3:c.150A= NP_005600.1:p.Arg50=
NM_005609.4:c.150A= MANE Select NP_005600.1:p.Arg50=