Canonical Allele Identifier: CA1978930068

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64759881T= , CM000673.2:g.64759881T=	GRCh38
NC_000011.9:g.64527353T= , CM000673.1:g.64527353T=	GRCh37
NC_000011.8:g.64283929T=	NCBI36
NG_013018.1:g.5835A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.18A= MANE Select	ENSP00000164139.3:p.Ser6=
ENST00000164139.3:c.18A=	ENSP00000164139.3:p.Ser6=
ENST00000377432.7:c.18A=	ENSP00000366650.3:p.Ser6=
NM_001164716.1:c.18A=	NP_001158188.1:p.Ser6=
NM_005609.2:c.18A=	NP_005600.1:p.Ser6=
NM_005609.3:c.18A=	NP_005600.1:p.Ser6=
NM_005609.4:c.18A= MANE Select	NP_005600.1:p.Ser6=