Canonical Allele Identifier: CA476797534

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112103951G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233228G>C , CM000673.2:g.112233228G>C	GRCh38
NC_000011.9:g.112103951G>C , CM000673.1:g.112103951G>C	GRCh37
NC_000011.8:g.111609161G>C	NCBI36
NG_008743.1:g.11864G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.309G>C MANE Select	ENSP00000280362.3:p.Val103=
ENST00000280362.7:c.309G>C	ENSP00000280362.3:p.Val103=
ENST00000524931.1:c.105G>C	ENSP00000434688.1:p.Val35=
ENST00000525803.1:c.*43G>C	ENSP00000431750.1:n.*43G>C
ENST00000527428.5:n.483G>C
ENST00000527635.1:n.350G>C
ENST00000528679.5:c.*118G>C	ENSP00000435895.1:n.*118G>C
ENST00000531175.1:n.260G>C
ENST00000531673.5:c.*118G>C	ENSP00000433469.1:n.*118G>C
NM_000317.2:c.309G>C	NP_000308.1:p.Val103=
XM_011542943.1:c.270G>C	XP_011541245.1:p.Val90=
NM_000317.3:c.309G>C MANE Select	NP_000308.1:p.Val103=