Canonical Allele Identifier: CA2000618397

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230279T= , CM000673.2:g.112230279T=	GRCh38
NC_000011.9:g.112101002T= , CM000673.1:g.112101002T=	GRCh37
NC_000011.8:g.111606212T=	NCBI36
NG_008743.1:g.8915T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.186+49T= MANE Select	ENSP00000280362.3:n.186+49T=
ENST00000280362.7:c.186+49T=	ENSP00000280362.3:n.186+49T=
ENST00000524931.1:c.-19+49T=	ENSP00000434688.1:n.-19+49T=
ENST00000525803.1:c.163+1606T=	ENSP00000431750.1:n.163+1606T=
ENST00000527428.5:n.14T=
ENST00000528679.5:c.164-347T=	ENSP00000435895.1:n.164-347T=
ENST00000531175.1:n.137+49T=
ENST00000531673.5:c.164-347T=	ENSP00000433469.1:n.164-347T=
NM_000317.2:c.186+49T=	NP_000308.1:n.186+49T=
XM_011542943.1:c.147+49T=	XP_011541245.1:n.147+49T=
NM_000317.3:c.186+49T= MANE Select	NP_000308.1:n.186+49T=