Canonical Allele Identifier: CA645554086

Gene: PTEN

Linked Data

• COSMIC: COSM4913

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960952_87960959del , CM000672.2:g.87960952_87960959del	GRCh38
NC_000010.10:g.89720709_89720716del , CM000672.1:g.89720709_89720716del	GRCh37
NC_000010.9:g.89710689_89710696del	NCBI36
NG_007466.2:g.102514_102521del , LRG_311:g.102514_102521del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.953_960del	ENSP00000514759.2:p.Ser318CysfsTer8
ENST00000710265.1:c.860_867del	ENSP00000518161.1:p.Ser287CysfsTer8
ENST00000472832.3:c.860_867del	ENSP00000483066.2:p.Ser287CysfsTer8
ENST00000688158.2:n.1595_1602del
ENST00000688922.2:c.*690_*697del	ENSP00000508742.2:n.*690_*697del
ENST00000700021.1:c.815_822del	ENSP00000514757.1:p.Ser272CysfsTer8
ENST00000700022.1:c.*199_*206del	ENSP00000514758.1:n.*199_*206del
ENST00000700023.1:n.2018_2025del
ENST00000700024.1:n.2252_2259del
ENST00000700025.1:n.1629_1636del
ENST00000700026.1:n.497_504del
ENST00000700029.1:c.787_794del
ENST00000706954.1:c.860_867del	ENSP00000516674.1:p.Ser287CysfsTer8
ENST00000706955.1:c.*895_*902del	ENSP00000516675.1:n.*895_*902del
ENST00000686459.1:c.*446_*453del	ENSP00000508909.1:n.*446_*453del
ENST00000688158.1:c.*971_*978del	ENSP00000509254.1:n.*971_*978del
ENST00000688308.1:c.860_867del	ENSP00000508752.1:p.Ser287CysfsTer8
ENST00000688922.1:c.781_788del
ENST00000693560.1:c.1379_1386del	ENSP00000509861.1:p.Ser460CysfsTer8
ENST00000371953.8:c.860_867del MANE Select	ENSP00000361021.3:p.Ser287CysfsTer8
ENST00000371953.7:c.860_867del	ENSP00000361021.3:p.Ser287CysfsTer8
ENST00000472832.2:c.287_294del	ENSP00000483066.1:p.Ser96CysfsTer8
NM_000314.5:c.860_867del	NP_000305.3:p.Ser287CysfsTer8
NM_000314.6:c.860_867del	NP_000305.3:p.Ser287CysfsTer8
NM_001304717.2:c.1379_1386del	NP_001291646.2:p.Ser460CysfsTer8
NM_001304718.1:c.269_276del	NP_001291647.1:p.Ser90CysfsTer8
XM_006717926.2:c.815_822del	XP_006717989.1:p.Ser272CysfsTer8
XM_011539981.1:c.860_867del	XP_011538283.1:p.Ser287CysfsTer8
XM_011539982.1:c.764_771del	XP_011538284.1:p.Ser255CysfsTer8
XR_945791.1:n.1430_1437del
NM_000314.7:c.860_867del	NP_000305.3:p.Ser287CysfsTer8
NM_001304717.5:c.1379_1386del	NP_001291646.4:p.Ser460CysfsTer8
NM_001304718.2:c.269_276del	NP_001291647.1:p.Ser90CysfsTer8
NM_000314.8:c.860_867del MANE Select	NP_000305.3:p.Ser287CysfsTer8