Canonical Allele Identifier: CA1978919029

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64747244A= , CM000673.2:g.64747244A=	GRCh38
NC_000011.9:g.64514716A= , CM000673.1:g.64514716A=	GRCh37
NC_000011.8:g.64271292A=	NCBI36
NG_007574.1:g.3213T= , LRG_100:g.3213T=
NG_013018.1:g.18472T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.2292T= MANE Select	ENSP00000164139.3:p.Asn764=
ENST00000164139.3:c.2292T=	ENSP00000164139.3:p.Asn764=
ENST00000377432.7:c.2028T=	ENSP00000366650.3:p.Asn676=
ENST00000483742.1:n.1645T=
NM_001164716.1:c.2028T=	NP_001158188.1:p.Asn676=
NM_005609.2:c.2292T=	NP_005600.1:p.Asn764=
NM_005609.3:c.2292T=	NP_005600.1:p.Asn764=
NM_005609.4:c.2292T= MANE Select	NP_005600.1:p.Asn764=