Canonical Allele Identifier: CA382628042

Gene: PTS

Linked Data

• MyVariant Identifiers: chr11:g.112104201G>A (hg19) ; chr11:g.112233478G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112233478G>A , CM000673.2:g.112233478G>A	GRCh38
NC_000011.9:g.112104201G>A , CM000673.1:g.112104201G>A	GRCh37
NC_000011.8:g.111609411G>A	NCBI36
NG_008743.1:g.12114G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.361G>A MANE Select	ENSP00000280362.3:p.Val121Ile
ENST00000280362.7:c.361G>A	ENSP00000280362.3:p.Val121Ile
ENST00000524931.1:c.157G>A	ENSP00000434688.1:p.Val53Ile
ENST00000525803.1:c.*95G>A	ENSP00000431750.1:n.*95G>A
ENST00000527428.5:n.488+245G>A
ENST00000527635.1:n.402G>A
ENST00000528679.5:c.*170G>A	ENSP00000435895.1:n.*170G>A
ENST00000531673.5:c.*123+245G>A	ENSP00000433469.1:n.*123+245G>A
NM_000317.2:c.361G>A	NP_000308.1:p.Val121Ile
XM_011542943.1:c.322G>A	XP_011541245.1:p.Val108Ile
NM_000317.3:c.361G>A MANE Select	NP_000308.1:p.Val121Ile