Canonical Allele Identifier: CA1978929991

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759819T= , CM000673.2:g.64759819T=	GRCh38
NC_000011.9:g.64527291T= , CM000673.1:g.64527291T=	GRCh37
NC_000011.8:g.64283867T=	NCBI36
NG_013018.1:g.5897A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.80A= MANE Select	ENSP00000164139.3:p.Glu27=
ENST00000164139.3:c.80A=	ENSP00000164139.3:p.Glu27=
ENST00000377432.7:c.80A=	ENSP00000366650.3:p.Glu27=
NM_001164716.1:c.80A=	NP_001158188.1:p.Glu27=
NM_005609.2:c.80A=	NP_005600.1:p.Glu27=
NM_005609.3:c.80A=	NP_005600.1:p.Glu27=
NM_005609.4:c.80A= MANE Select	NP_005600.1:p.Glu27=