Canonical Allele Identifier: CA1978913494

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64750505A= , CM000673.2:g.64750505A=	GRCh38
NC_000011.9:g.64517977A= , CM000673.1:g.64517977A=	GRCh37
NC_000011.8:g.64274553A=	NCBI36
NG_013018.1:g.15211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2048T= MANE Select	ENSP00000164139.3:p.Met683=
ENST00000164139.3:c.2048T=	ENSP00000164139.3:p.Met683=
ENST00000377432.7:c.1784T=	ENSP00000366650.3:p.Met595=
NM_001164716.1:c.1784T=	NP_001158188.1:p.Met595=
NM_005609.2:c.2048T=	NP_005600.1:p.Met683=
NM_005609.3:c.2048T=	NP_005600.1:p.Met683=
NM_005609.4:c.2048T= MANE Select	NP_005600.1:p.Met683=