Canonical Allele Identifier: CA2000619893

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233371A= , CM000673.2:g.112233371A=	GRCh38
NC_000011.9:g.112104094A= , CM000673.1:g.112104094A=	GRCh37
NC_000011.8:g.111609304A=	NCBI36
NG_008743.1:g.12007A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.315-61A= MANE Select	ENSP00000280362.3:n.315-61A=
ENST00000280362.7:c.315-61A=	ENSP00000280362.3:n.315-61A=
ENST00000524931.1:c.111-61A=	ENSP00000434688.1:n.111-61A=
ENST00000525803.1:c.*49-61A=	ENSP00000431750.1:n.*49-61A=
ENST00000527428.5:n.488+138A=
ENST00000527635.1:n.356-61A=
ENST00000528679.5:c.*124-61A=	ENSP00000435895.1:n.*124-61A=
ENST00000531175.1:n.403A=
ENST00000531673.5:c.*123+138A=	ENSP00000433469.1:n.*123+138A=
NM_000317.2:c.315-61A=	NP_000308.1:n.315-61A=
XM_011542943.1:c.276-61A=	XP_011541245.1:n.276-61A=
NM_000317.3:c.315-61A= MANE Select	NP_000308.1:n.315-61A=