Canonical Allele Identifier: CA1978918994

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747227T= , CM000673.2:g.64747227T=	GRCh38
NC_000011.9:g.64514699T= , CM000673.1:g.64514699T=	GRCh37
NC_000011.8:g.64271275T=	NCBI36
NG_007574.1:g.3230A= , LRG_100:g.3230A=
NG_013018.1:g.18489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2309A= MANE Select	ENSP00000164139.3:p.Asp770=
ENST00000164139.3:c.2309A=	ENSP00000164139.3:p.Asp770=
ENST00000377432.7:c.2045A=	ENSP00000366650.3:p.Asp682=
ENST00000483742.1:n.1662A=
NM_001164716.1:c.2045A=	NP_001158188.1:p.Asp682=
NM_005609.2:c.2309A=	NP_005600.1:p.Asp770=
NM_005609.3:c.2309A=	NP_005600.1:p.Asp770=
NM_005609.4:c.2309A= MANE Select	NP_005600.1:p.Asp770=