Canonical Allele Identifier: CA1978920282

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64753126G= , CM000673.2:g.64753126G=	GRCh38
NC_000011.9:g.64520598G= , CM000673.1:g.64520598G=	GRCh37
NC_000011.8:g.64277174G=	NCBI36
NG_013018.1:g.12590C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.1465C= MANE Select	ENSP00000164139.3:p.Pro489=
ENST00000164139.3:c.1465C=	ENSP00000164139.3:p.Pro489=
ENST00000377432.7:c.1201C=	ENSP00000366650.3:p.Pro401=
NM_001164716.1:c.1201C=	NP_001158188.1:p.Pro401=
NM_005609.2:c.1465C=	NP_005600.1:p.Pro489=
NM_005609.3:c.1465C=	NP_005600.1:p.Pro489=
NM_005609.4:c.1465C= MANE Select	NP_005600.1:p.Pro489=