Canonical Allele Identifier: CA1978920298

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64753129T= , CM000673.2:g.64753129T=	GRCh38
NC_000011.9:g.64520601T= , CM000673.1:g.64520601T=	GRCh37
NC_000011.8:g.64277177T=	NCBI36
NG_013018.1:g.12587A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000164139.4:c.1462A= MANE Select	ENSP00000164139.3:p.Thr488=
ENST00000164139.3:c.1462A=	ENSP00000164139.3:p.Thr488=
ENST00000377432.7:c.1198A=	ENSP00000366650.3:p.Thr400=
NM_001164716.1:c.1198A=	NP_001158188.1:p.Thr400=
NM_005609.2:c.1462A=	NP_005600.1:p.Thr488=
NM_005609.3:c.1462A=	NP_005600.1:p.Thr488=
NM_005609.4:c.1462A= MANE Select	NP_005600.1:p.Thr488=