Canonical Allele Identifier: CA2000619821

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233211C= , CM000673.2:g.112233211C=	GRCh38
NC_000011.9:g.112103934C= , CM000673.1:g.112103934C=	GRCh37
NC_000011.8:g.111609144C=	NCBI36
NG_008743.1:g.11847C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.292C= MANE Select	ENSP00000280362.3:p.Pro98=
ENST00000280362.7:c.292C=	ENSP00000280362.3:p.Pro98=
ENST00000524931.1:c.88C=	ENSP00000434688.1:p.Pro30=
ENST00000525803.1:c.*26C=	ENSP00000431750.1:n.*26C=
ENST00000527428.5:n.466C=
ENST00000527635.1:n.333C=
ENST00000528679.5:c.*101C=	ENSP00000435895.1:n.*101C=
ENST00000531175.1:n.243C=
ENST00000531673.5:c.*101C=	ENSP00000433469.1:n.*101C=
NM_000317.2:c.292C=	NP_000308.1:p.Pro98=
XM_011542943.1:c.253C=	XP_011541245.1:p.Pro85=
NM_000317.3:c.292C= MANE Select	NP_000308.1:p.Pro98=