Canonical Allele Identifier: CA2000619762

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233102A= , CM000673.2:g.112233102A=	GRCh38
NC_000011.9:g.112103825A= , CM000673.1:g.112103825A=	GRCh37
NC_000011.8:g.111609035A=	NCBI36
NG_008743.1:g.11738A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.244-61A= MANE Select	ENSP00000280362.3:n.244-61A=
ENST00000280362.7:c.244-61A=	ENSP00000280362.3:n.244-61A=
ENST00000524931.1:c.40-61A=	ENSP00000434688.1:n.40-61A=
ENST00000525803.1:c.164-61A=	ENSP00000431750.1:n.164-61A=
ENST00000527428.5:n.418-61A=
ENST00000527635.1:n.285-61A=
ENST00000528679.5:c.*53-61A=	ENSP00000435895.1:n.*53-61A=
ENST00000531175.1:n.195-61A=
ENST00000531673.5:c.*53-61A=	ENSP00000433469.1:n.*53-61A=
NM_000317.2:c.244-61A=	NP_000308.1:n.244-61A=
XM_011542943.1:c.205-61A=	XP_011541245.1:n.205-61A=
NM_000317.3:c.244-61A= MANE Select	NP_000308.1:n.244-61A=