Canonical Allele Identifier: CA2000617620

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228605G= , CM000673.2:g.112228605G=	GRCh38
NC_000011.9:g.112099328G= , CM000673.1:g.112099328G=	GRCh37
NC_000011.8:g.111604538G=	NCBI36
NG_008743.1:g.7241G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.95G= MANE Select	ENSP00000280362.3:p.Ser32=
ENST00000280362.7:c.95G=	ENSP00000280362.3:p.Ser32=
ENST00000524931.1:c.-110G=	ENSP00000434688.1:n.-110G=
ENST00000525645.1:n.170G=
ENST00000525803.1:c.95G=	ENSP00000431750.1:p.Ser32=
ENST00000528679.5:c.95G=	ENSP00000435895.1:p.Ser32=
ENST00000531673.5:c.95G=	ENSP00000433469.1:p.Ser32=
NM_000317.2:c.95G=	NP_000308.1:p.Ser32=
NM_000317.3:c.95G= MANE Select	NP_000308.1:p.Ser32=