Canonical Allele Identifier: CA1926142813

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863246_87863247delinsTC , CM000672.2:g.87863246_87863247delinsTC GRCh38
NC_000010.10:g.89623003_89623004delinsTC , CM000672.1:g.89623003_89623004delinsTC GRCh37
NC_000010.9:g.89612983_89612984delinsTC NCBI36
NG_007466.2:g.4809_4810delinsTC , LRG_311:g.4809_4810delinsTC
NG_033079.1:g.5191_5192delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+604_-17+605delinsTC (PTEN) ENSP00000516674.1:n.-17+604_-17+605delinsTC
ENST00000688308.1:c.-17+133_-17+134delinsTC (PTEN) ENSP00000508752.1:n.-17+133_-17+134delinsTC
ENST00000445946.5:c.-760_-759delinsGA (KLLN) MANE Select ENSP00000392204.2:n.-760_-759delinsGA
ENST00000371953.7:c.-1224_-1223delinsTC (PTEN) ENSP00000361021.3:n.-1224_-1223delinsTC
ENST00000445946.3:c.-760_-759delinsGA (KLLN) ENSP00000392204.2:n.-760_-759delinsGA
NM_001126049.1:c.-760_-759delinsGA (KLLN) NP_001119521.1:n.-760_-759delinsGA
NM_001126049.2:c.-760_-759delinsGA (KLLN) MANE Select NP_001119521.1:n.-760_-759delinsGA