Canonical Allele Identifier: CA1978917732

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64751926T= , CM000673.2:g.64751926T=	GRCh38
NC_000011.9:g.64519398T= , CM000673.1:g.64519398T=	GRCh37
NC_000011.8:g.64275974T=	NCBI36
NG_013018.1:g.13790A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.1766A= MANE Select	ENSP00000164139.3:p.Asn589=
ENST00000164139.3:c.1766A=	ENSP00000164139.3:p.Asn589=
ENST00000377432.7:c.1502A=	ENSP00000366650.3:p.Asn501=
ENST00000462303.1:n.90A=
NM_001164716.1:c.1502A=	NP_001158188.1:p.Asn501=
NM_005609.2:c.1766A=	NP_005600.1:p.Asn589=
NM_005609.3:c.1766A=	NP_005600.1:p.Asn589=
NM_005609.4:c.1766A= MANE Select	NP_005600.1:p.Asn589=