Canonical Allele Identifier: CA382627751

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112103886G>C (hg19) ; chr11:g.112233163G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233163G>C , CM000673.2:g.112233163G>C	GRCh38
NC_000011.9:g.112103886G>C , CM000673.1:g.112103886G>C	GRCh37
NC_000011.8:g.111609096G>C	NCBI36
NG_008743.1:g.11799G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.244G>C MANE Select	ENSP00000280362.3:p.Glu82Gln
ENST00000280362.7:c.244G>C	ENSP00000280362.3:p.Glu82Gln
ENST00000524931.1:c.40G>C	ENSP00000434688.1:p.Glu14Gln
ENST00000525803.1:c.164G>C	ENSP00000431750.1:p.Gly55Ala
ENST00000527428.5:n.418G>C
ENST00000527635.1:n.285G>C
ENST00000528679.5:c.*53G>C	ENSP00000435895.1:n.*53G>C
ENST00000531175.1:n.195G>C
ENST00000531673.5:c.*53G>C	ENSP00000433469.1:n.*53G>C
NM_000317.2:c.244G>C	NP_000308.1:p.Glu82Gln
XM_011542943.1:c.205G>C	XP_011541245.1:p.Glu69Gln
NM_000317.3:c.244G>C MANE Select	NP_000308.1:p.Glu82Gln