Canonical Allele Identifier: CA2610045344

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863042_87863043insTTTTAATGATACG , CM000672.2:g.87863042_87863043insTTTTAATGATACG GRCh38
NC_000010.10:g.89622799_89622800insTTTTAATGATACG , CM000672.1:g.89622799_89622800insTTTTAATGATACG GRCh37
NC_000010.9:g.89612779_89612780insTTTTAATGATACG NCBI36
NG_007466.2:g.4605_4606insTTTTAATGATACG , LRG_311:g.4605_4606insTTTTAATGATACG
NG_033079.1:g.5395_5396insCGTATCATTAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+400_-17+401insTTTTAATGATACG (PTEN) ENSP00000516674.1:n.-17+400_-17+401insTTTTAATGATACG
ENST00000688308.1:c.-88_-87insTTTTAATGATACG (PTEN) ENSP00000508752.1:n.-88_-87insTTTTAATGATACG
ENST00000445946.5:c.-556_-555insCGTATCATTAAAA (KLLN) MANE Select ENSP00000392204.2:n.-556_-555insCGTATCATTAAAA
ENST00000445946.3:c.-556_-555insCGTATCATTAAAA (KLLN) ENSP00000392204.2:n.-556_-555insCGTATCATTAAAA
NM_001126049.1:c.-556_-555insCGTATCATTAAAA (KLLN) NP_001119521.1:n.-556_-555insCGTATCATTAAAA
NM_001126049.2:c.-556_-555insCGTATCATTAAAA (KLLN) MANE Select NP_001119521.1:n.-556_-555insCGTATCATTAAAA