Canonical Allele Identifier: CA476797523

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112103933G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233210G>T , CM000673.2:g.112233210G>T	GRCh38
NC_000011.9:g.112103933G>T , CM000673.1:g.112103933G>T	GRCh37
NC_000011.8:g.111609143G>T	NCBI36
NG_008743.1:g.11846G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280362.8:c.291G>T MANE Select	ENSP00000280362.3:p.Val97=
ENST00000280362.7:c.291G>T	ENSP00000280362.3:p.Val97=
ENST00000524931.1:c.87G>T	ENSP00000434688.1:p.Val29=
ENST00000525803.1:c.*25G>T	ENSP00000431750.1:n.*25G>T
ENST00000527428.5:n.465G>T
ENST00000527635.1:n.332G>T
ENST00000528679.5:c.*100G>T	ENSP00000435895.1:n.*100G>T
ENST00000531175.1:n.242G>T
ENST00000531673.5:c.*100G>T	ENSP00000433469.1:n.*100G>T
NM_000317.2:c.291G>T	NP_000308.1:p.Val97=
XM_011542943.1:c.252G>T	XP_011541245.1:p.Val84=
NM_000317.3:c.291G>T MANE Select	NP_000308.1:p.Val97=