Canonical Allele Identifier: CA2610045399

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863066_87863067insGAGA , CM000672.2:g.87863066_87863067insGAGA GRCh38
NC_000010.10:g.89622823_89622824insGAGA , CM000672.1:g.89622823_89622824insGAGA GRCh37
NC_000010.9:g.89612803_89612804insGAGA NCBI36
NG_007466.2:g.4629_4630insGAGA , LRG_311:g.4629_4630insGAGA
NG_033079.1:g.5371_5372insTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+424_-17+425insGAGA (PTEN) ENSP00000516674.1:n.-17+424_-17+425insGAGA
ENST00000688308.1:c.-64_-63insGAGA (PTEN) ENSP00000508752.1:n.-64_-63insGAGA
ENST00000445946.5:c.-580_-579insTCTC (KLLN) MANE Select ENSP00000392204.2:n.-580_-579insTCTC
ENST00000445946.3:c.-580_-579insTCTC (KLLN) ENSP00000392204.2:n.-580_-579insTCTC
NM_001126049.1:c.-580_-579insTCTC (KLLN) NP_001119521.1:n.-580_-579insTCTC
NM_001126049.2:c.-580_-579insTCTC (KLLN) MANE Select NP_001119521.1:n.-580_-579insTCTC