Canonical Allele Identifier: CA1978928066

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64758242T= , CM000673.2:g.64758242T=	GRCh38
NC_000011.9:g.64525714T= , CM000673.1:g.64525714T=	GRCh37
NC_000011.8:g.64282290T=	NCBI36
NG_013018.1:g.7474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.528+4A= MANE Select	ENSP00000164139.3:n.528+4A=
ENST00000164139.3:c.528+4A=	ENSP00000164139.3:n.528+4A=
ENST00000377432.7:c.264+4A=	ENSP00000366650.3:n.264+4A=
NM_001164716.1:c.264+4A=	NP_001158188.1:n.264+4A=
NM_005609.2:c.528+4A=	NP_005600.1:n.528+4A=
NM_005609.3:c.528+4A=	NP_005600.1:n.528+4A=
NM_005609.4:c.528+4A= MANE Select	NP_005600.1:n.528+4A=