Canonical Allele Identifier: CA2610044788
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925447_87925449dup , CM000672.2:g.87925447_87925449dup GRCh38
NC_000010.10:g.89685204_89685206dup , CM000672.1:g.89685204_89685206dup GRCh37
NC_000010.9:g.89675184_89675186dup NCBI36
NG_007466.2:g.67009_67011dup , LRG_311:g.67009_67011dup

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.165-66_165-64dup ENSP00000514759.2:n.165-66_165-64dup
ENST00000710265.1:c.165-66_165-64dup ENSP00000518161.1:n.165-66_165-64dup
ENST00000472832.3:c.165-66_165-64dup ENSP00000483066.2:n.165-66_165-64dup
ENST00000688158.2:n.900-66_900-64dup
ENST00000688922.2:c.165-66_165-64dup ENSP00000508742.2:n.165-66_165-64dup
ENST00000700021.1:c.165-5599_165-5597dup ENSP00000514757.1:n.165-5599_165-5597dup
ENST00000700022.1:c.165-66_165-64dup ENSP00000514758.1:n.165-66_165-64dup
ENST00000706954.1:c.165-66_165-64dup ENSP00000516674.1:n.165-66_165-64dup
ENST00000706955.1:c.*200-66_*200-64dup ENSP00000516675.1:n.*200-66_*200-64dup
ENST00000686459.1:c.165-66_165-64dup ENSP00000508909.1:n.165-66_165-64dup
ENST00000688158.1:c.*276-66_*276-64dup ENSP00000509254.1:n.*276-66_*276-64dup
ENST00000688308.1:c.165-66_165-64dup ENSP00000508752.1:n.165-66_165-64dup
ENST00000688922.1:c.34-66_34-64dup
ENST00000693560.1:c.684-66_684-64dup ENSP00000509861.1:n.684-66_684-64dup
ENST00000371953.8:c.165-66_165-64dup MANE Select ENSP00000361021.3:n.165-66_165-64dup
ENST00000371953.7:c.165-66_165-64dup ENSP00000361021.3:n.165-66_165-64dup
ENST00000610634.1:c.63-66_63-64dup ENSP00000477517.1:n.63-66_63-64dup
NM_000314.5:c.165-66_165-64dup NP_000305.3:n.165-66_165-64dup
NM_000314.6:c.165-66_165-64dup NP_000305.3:n.165-66_165-64dup
NM_001304717.2:c.684-66_684-64dup NP_001291646.2:n.684-66_684-64dup
NM_001304718.1:c.-541-5599_-541-5597dup NP_001291647.1:n.-541-5599_-541-5597dup
XM_006717926.2:c.165-5599_165-5597dup XP_006717989.1:n.165-5599_165-5597dup
XM_011539981.1:c.165-66_165-64dup XP_011538283.1:n.165-66_165-64dup
XM_011539982.1:c.69-66_69-64dup XP_011538284.1:n.69-66_69-64dup
XR_945789.1:n.877-66_877-64dup
XR_945790.1:n.877-66_877-64dup
XR_945791.1:n.877-66_877-64dup
NM_000314.7:c.165-66_165-64dup NP_000305.3:n.165-66_165-64dup
NM_001304717.5:c.684-66_684-64dup NP_001291646.4:n.684-66_684-64dup
NM_001304718.2:c.-541-5599_-541-5597dup NP_001291647.1:n.-541-5599_-541-5597dup
NM_000314.8:c.165-66_165-64dup MANE Select NP_000305.3:n.165-66_165-64dup