Canonical Allele Identifier: CA1978916078

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64751378T= , CM000673.2:g.64751378T=	GRCh38
NC_000011.9:g.64518850T= , CM000673.1:g.64518850T=	GRCh37
NC_000011.8:g.64275426T=	NCBI36
NG_013018.1:g.14338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.1916A= MANE Select	ENSP00000164139.3:p.Asp639=
ENST00000164139.3:c.1916A=	ENSP00000164139.3:p.Asp639=
ENST00000377432.7:c.1652A=	ENSP00000366650.3:p.Asp551=
ENST00000462303.1:n.240A=
NM_001164716.1:c.1652A=	NP_001158188.1:p.Asp551=
NM_005609.2:c.1916A=	NP_005600.1:p.Asp639=
NM_005609.3:c.1916A=	NP_005600.1:p.Asp639=
NM_005609.4:c.1916A= MANE Select	NP_005600.1:p.Asp639=