Canonical Allele Identifier: CA2616001586

Gene: PTS

Linked Data

• gnomAD v4: 11-112233294-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233294T>C , CM000673.2:g.112233294T>C	GRCh38
NC_000011.9:g.112104017T>C , CM000673.1:g.112104017T>C	GRCh37
NC_000011.8:g.111609227T>C	NCBI36
NG_008743.1:g.11930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.314+61T>C MANE Select	ENSP00000280362.3:n.314+61T>C
ENST00000280362.7:c.314+61T>C	ENSP00000280362.3:n.314+61T>C
ENST00000524931.1:c.110+61T>C	ENSP00000434688.1:n.110+61T>C
ENST00000525803.1:c.*48+61T>C	ENSP00000431750.1:n.*48+61T>C
ENST00000527428.5:n.488+61T>C
ENST00000527635.1:n.355+61T>C
ENST00000528679.5:c.*123+61T>C	ENSP00000435895.1:n.*123+61T>C
ENST00000531175.1:n.326T>C
ENST00000531673.5:c.*123+61T>C	ENSP00000433469.1:n.*123+61T>C
NM_000317.2:c.314+61T>C	NP_000308.1:n.314+61T>C
XM_011542943.1:c.275+61T>C	XP_011541245.1:n.275+61T>C
NM_000317.3:c.314+61T>C MANE Select	NP_000308.1:n.314+61T>C