Canonical Allele Identifier: CA2000617658

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112228689A= , CM000673.2:g.112228689A=	GRCh38
NC_000011.9:g.112099412A= , CM000673.1:g.112099412A=	GRCh37
NC_000011.8:g.111604622A=	NCBI36
NG_008743.1:g.7325A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.163+16A= MANE Select	ENSP00000280362.3:n.163+16A=
ENST00000280362.7:c.163+16A=	ENSP00000280362.3:n.163+16A=
ENST00000524931.1:c.-42+16A=	ENSP00000434688.1:n.-42+16A=
ENST00000525645.1:n.254A=
ENST00000525803.1:c.163+16A=	ENSP00000431750.1:n.163+16A=
ENST00000528679.5:c.163+16A=	ENSP00000435895.1:n.163+16A=
ENST00000531673.5:c.163+16A=	ENSP00000433469.1:n.163+16A=
NM_000317.2:c.163+16A=	NP_000308.1:n.163+16A=
XM_011542943.1:c.-674A=	XP_011541245.1:n.-674A=
NM_000317.3:c.163+16A= MANE Select	NP_000308.1:n.163+16A=