Canonical Allele Identifier: CA1978928132

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64758269G= , CM000673.2:g.64758269G=	GRCh38
NC_000011.9:g.64525741G= , CM000673.1:g.64525741G=	GRCh37
NC_000011.8:g.64282317G=	NCBI36
NG_013018.1:g.7447C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.505C= MANE Select	ENSP00000164139.3:p.Gln169=
ENST00000164139.3:c.505C=	ENSP00000164139.3:p.Gln169=
ENST00000377432.7:c.244-3C=	ENSP00000366650.3:n.244-3C=
NM_001164716.1:c.244-3C=	NP_001158188.1:n.244-3C=
NM_005609.2:c.505C=	NP_005600.1:p.Gln169=
NM_005609.3:c.505C=	NP_005600.1:p.Gln169=
NM_005609.4:c.505C= MANE Select	NP_005600.1:p.Gln169=