Canonical Allele Identifier: CA1978918559

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64746981T= , CM000673.2:g.64746981T=	GRCh38
NC_000011.9:g.64514453T= , CM000673.1:g.64514453T=	GRCh37
NC_000011.8:g.64271029T=	NCBI36
NG_007574.1:g.3476A= , LRG_100:g.3476A=
NG_013018.1:g.18735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2319A= MANE Select	ENSP00000164139.3:p.Lys773=
ENST00000164139.3:c.2319A=	ENSP00000164139.3:p.Lys773=
ENST00000377432.7:c.2055A=	ENSP00000366650.3:p.Lys685=
ENST00000483742.1:n.1672A=
NM_001164716.1:c.2055A=	NP_001158188.1:p.Lys685=
NM_005609.2:c.2319A=	NP_005600.1:p.Lys773=
NM_005609.3:c.2319A=	NP_005600.1:p.Lys773=
NM_005609.4:c.2319A= MANE Select	NP_005600.1:p.Lys773=