Canonical Allele Identifier: CA2579927020
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933049_87933051del , CM000672.2:g.87933049_87933051del GRCh38
NC_000010.10:g.89692806_89692808del , CM000672.1:g.89692806_89692808del GRCh37
NC_000010.9:g.89682786_89682788del NCBI36
NG_007466.2:g.74611_74613del , LRG_311:g.74611_74613del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.290_292del ENSP00000514759.2:p.Gln97del
ENST00000710265.1:c.290_292del ENSP00000518161.1:p.Gln97del
ENST00000472832.3:c.290_292del ENSP00000483066.2:p.Gln97del
ENST00000688158.2:n.1025_1027del
ENST00000688922.2:c.*120_*122del ENSP00000508742.2:n.*120_*122del
ENST00000700021.1:c.245_247del ENSP00000514757.1:p.Gln82del
ENST00000700022.1:c.290_292del ENSP00000514758.1:p.Gln97del
ENST00000700029.1:c.124_126del
ENST00000706954.1:c.290_292del ENSP00000516674.1:p.Gln97del
ENST00000706955.1:c.*325_*327del ENSP00000516675.1:n.*325_*327del
ENST00000686459.1:c.290_292del ENSP00000508909.1:p.Gln97del
ENST00000688158.1:c.*401_*403del ENSP00000509254.1:n.*401_*403del
ENST00000688308.1:c.290_292del ENSP00000508752.1:p.Gln97del
ENST00000688922.1:c.211_213del
ENST00000693560.1:c.809_811del ENSP00000509861.1:p.Gln270del
ENST00000371953.8:c.290_292del MANE Select ENSP00000361021.3:p.Gln97del
ENST00000371953.7:c.290_292del ENSP00000361021.3:p.Gln97del
ENST00000498703.1:n.116_118del
ENST00000610634.1:c.188_190del ENSP00000477517.1:p.Gln63del
NM_000314.5:c.290_292del NP_000305.3:p.Gln97del
NM_000314.6:c.290_292del NP_000305.3:p.Gln97del
NM_001304717.2:c.809_811del NP_001291646.2:p.Gln270del
NM_001304718.1:c.-461_-459del NP_001291647.1:n.-461_-459del
XM_006717926.2:c.245_247del XP_006717989.1:p.Gln82del
XM_011539981.1:c.290_292del XP_011538283.1:p.Gln97del
XM_011539982.1:c.194_196del XP_011538284.1:p.Gln65del
XR_945789.1:n.1002_1004del
XR_945790.1:n.1002_1004del
XR_945791.1:n.1002_1004del
NM_000314.7:c.290_292del NP_000305.3:p.Gln97del
NM_001304717.5:c.809_811del NP_001291646.4:p.Gln270del
NM_001304718.2:c.-461_-459del NP_001291647.1:n.-461_-459del
NM_000314.8:c.290_292del MANE Select NP_000305.3:p.Gln97del