Canonical Allele Identifier: CA2000617621

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228606T= , CM000673.2:g.112228606T=	GRCh38
NC_000011.9:g.112099329T= , CM000673.1:g.112099329T=	GRCh37
NC_000011.8:g.111604539T=	NCBI36
NG_008743.1:g.7242T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.96T= MANE Select	ENSP00000280362.3:p.Ser32=
ENST00000280362.7:c.96T=	ENSP00000280362.3:p.Ser32=
ENST00000524931.1:c.-109T=	ENSP00000434688.1:n.-109T=
ENST00000525645.1:n.171T=
ENST00000525803.1:c.96T=	ENSP00000431750.1:p.Ser32=
ENST00000528679.5:c.96T=	ENSP00000435895.1:p.Ser32=
ENST00000531673.5:c.96T=	ENSP00000433469.1:p.Ser32=
NM_000317.2:c.96T=	NP_000308.1:p.Ser32=
NM_000317.3:c.96T= MANE Select	NP_000308.1:p.Ser32=