Canonical Allele Identifier: CA2000619825

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233216C= , CM000673.2:g.112233216C=	GRCh38
NC_000011.9:g.112103939C= , CM000673.1:g.112103939C=	GRCh37
NC_000011.8:g.111609149C=	NCBI36
NG_008743.1:g.11852C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000317.3:c.297C= MANE Select	NP_000308.1:p.Tyr99=
ENST00000280362.8:c.297C= MANE Select	ENSP00000280362.3:p.Tyr99=
NM_000317.2:c.297C=	NP_000308.1:p.Tyr99=
ENST00000280362.7:c.297C=	ENSP00000280362.3:p.Tyr99=
ENST00000524931.1:c.93C=	ENSP00000434688.1:p.Tyr31=
ENST00000525803.1:c.*31C=	ENSP00000431750.1:n.*31C=
ENST00000527428.5:n.471C=
ENST00000527635.1:n.338C=
ENST00000528679.5:c.*106C=	ENSP00000435895.1:n.*106C=
ENST00000531175.1:n.248C=
ENST00000531673.5:c.*106C=	ENSP00000433469.1:n.*106C=
XM_011542943.1:c.258C=	XP_011541245.1:p.Tyr86=