Canonical Allele Identifier: CA1978921114

Gene: PYGM

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64753547T= , CM000673.2:g.64753547T=	GRCh38
NC_000011.9:g.64521019T= , CM000673.1:g.64521019T=	GRCh37
NC_000011.8:g.64277595T=	NCBI36
NG_013018.1:g.12169A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.1375A= MANE Select	ENSP00000164139.3:p.Ile459=
ENST00000164139.3:c.1375A=	ENSP00000164139.3:p.Ile459=
ENST00000377432.7:c.1111A=	ENSP00000366650.3:p.Ile371=
NM_001164716.1:c.1111A=	NP_001158188.1:p.Ile371=
NM_005609.2:c.1375A=	NP_005600.1:p.Ile459=
NM_005609.3:c.1375A=	NP_005600.1:p.Ile459=
NM_005609.4:c.1375A= MANE Select	NP_005600.1:p.Ile459=