Canonical Allele Identifier: CA2000618566

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230601A= , CM000673.2:g.112230601A=	GRCh38
NC_000011.9:g.112101324A= , CM000673.1:g.112101324A=	GRCh37
NC_000011.8:g.111606534A=	NCBI36
NG_008743.1:g.9237A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.187-25A= MANE Select	ENSP00000280362.3:n.187-25A=
ENST00000280362.7:c.187-25A=	ENSP00000280362.3:n.187-25A=
ENST00000524931.1:c.-18-25A=	ENSP00000434688.1:n.-18-25A=
ENST00000525803.1:c.163+1928A=	ENSP00000431750.1:n.163+1928A=
ENST00000527428.5:n.336A=
ENST00000527635.1:n.203A=
ENST00000528679.5:c.164-25A=	ENSP00000435895.1:n.164-25A=
ENST00000531175.1:n.138-25A=
ENST00000531673.5:c.164-25A=	ENSP00000433469.1:n.164-25A=
NM_000317.2:c.187-25A=	NP_000308.1:n.187-25A=
XM_011542943.1:c.148-25A=	XP_011541245.1:n.148-25A=
NM_000317.3:c.187-25A= MANE Select	NP_000308.1:n.187-25A=