Canonical Allele Identifier: CA1926142719

Linked Data

dbSNP Id: rs1858312693

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863115_87863116insTTTGT , CM000672.2:g.87863115_87863116insTTTGT GRCh38
NC_000010.10:g.89622872_89622873insTTTGT , CM000672.1:g.89622872_89622873insTTTGT GRCh37
NC_000010.9:g.89612852_89612853insTTTGT NCBI36
NG_007466.2:g.4678_4679insTTTGT , LRG_311:g.4678_4679insTTTGT
NG_033079.1:g.5324_5325insAAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+473_-17+474insTTTGT (PTEN) ENSP00000516674.1:n.-17+473_-17+474insTTTGT
ENST00000688308.1:c.-17+2_-17+3insTTTGT (PTEN) ENSP00000508752.1:n.-17+2_-17+3insTTTGT
ENST00000445946.5:c.-627_-626insAAAAC (KLLN) MANE Select ENSP00000392204.2:n.-627_-626insAAAAC
ENST00000371953.7:c.-1355_-1354insTTTGT (PTEN) ENSP00000361021.3:n.-1355_-1354insTTTGT
ENST00000445946.3:c.-627_-626insAAAAC (KLLN) ENSP00000392204.2:n.-627_-626insAAAAC
NM_001126049.1:c.-627_-626insAAAAC (KLLN) NP_001119521.1:n.-627_-626insAAAAC
NM_001126049.2:c.-627_-626insAAAAC (KLLN) MANE Select NP_001119521.1:n.-627_-626insAAAAC