Canonical Allele Identifier: CA2000618564

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230598G= , CM000673.2:g.112230598G=	GRCh38
NC_000011.9:g.112101321G= , CM000673.1:g.112101321G=	GRCh37
NC_000011.8:g.111606531G=	NCBI36
NG_008743.1:g.9234G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.187-28G= MANE Select	ENSP00000280362.3:n.187-28G=
ENST00000280362.7:c.187-28G=	ENSP00000280362.3:n.187-28G=
ENST00000524931.1:c.-18-28G=	ENSP00000434688.1:n.-18-28G=
ENST00000525803.1:c.163+1925G=	ENSP00000431750.1:n.163+1925G=
ENST00000527428.5:n.333G=
ENST00000527635.1:n.200G=
ENST00000528679.5:c.164-28G=	ENSP00000435895.1:n.164-28G=
ENST00000531175.1:n.138-28G=
ENST00000531673.5:c.164-28G=	ENSP00000433469.1:n.164-28G=
NM_000317.2:c.187-28G=	NP_000308.1:n.187-28G=
XM_011542943.1:c.148-28G=	XP_011541245.1:n.148-28G=
NM_000317.3:c.187-28G= MANE Select	NP_000308.1:n.187-28G=