Canonical Allele Identifier: CA645553819

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933120_87933194del , CM000672.2:g.87933120_87933194del	GRCh38
NC_000010.10:g.89692877_89692951del , CM000672.1:g.89692877_89692951del	GRCh37
NC_000010.9:g.89682857_89682931del	NCBI36
NG_007466.2:g.74682_74756del , LRG_311:g.74682_74756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.361_435del	ENSP00000514759.2:p.Ala121_Phe145del
ENST00000710265.1:c.361_435del	ENSP00000518161.1:p.Ala121_Phe145del
ENST00000472832.3:c.361_435del	ENSP00000483066.2:p.Ala121_Phe145del
ENST00000688158.2:n.1096_1170del
ENST00000688922.2:c.*191_*265del	ENSP00000508742.2:n.*191_*265del
ENST00000700021.1:c.316_390del	ENSP00000514757.1:p.Ala106_Phe130del
ENST00000700022.1:c.361_435del	ENSP00000514758.1:p.Ala121_Phe145del
ENST00000700029.1:c.195_269del
ENST00000706954.1:c.361_435del	ENSP00000516674.1:p.Ala121_Phe145del
ENST00000706955.1:c.*396_*470del	ENSP00000516675.1:n.*396_*470del
ENST00000686459.1:c.361_435del	ENSP00000508909.1:p.Ala121_Phe145del
ENST00000688158.1:c.*472_*546del	ENSP00000509254.1:n.*472_*546del
ENST00000688308.1:c.361_435del	ENSP00000508752.1:p.Ala121_Phe145del
ENST00000688922.1:c.282_356del
ENST00000693560.1:c.880_954del	ENSP00000509861.1:p.Ala294_Phe318del
ENST00000371953.8:c.361_435del MANE Select	ENSP00000361021.3:p.Ala121_Phe145del
ENST00000371953.7:c.361_435del	ENSP00000361021.3:p.Ala121_Phe145del
ENST00000498703.1:n.187_261del
ENST00000610634.1:c.259_333del	ENSP00000477517.1:p.Ala87_Phe111del
NM_000314.5:c.361_435del	NP_000305.3:p.Ala121_Phe145del
NM_000314.6:c.361_435del	NP_000305.3:p.Ala121_Phe145del
NM_001304717.2:c.880_954del	NP_001291646.2:p.Ala294_Phe318del
NM_001304718.1:c.-390_-316del	NP_001291647.1:n.-390_-316del
XM_006717926.2:c.316_390del	XP_006717989.1:p.Ala106_Phe130del
XM_011539981.1:c.361_435del	XP_011538283.1:p.Ala121_Phe145del
XM_011539982.1:c.265_339del	XP_011538284.1:p.Ala89_Phe113del
XR_945789.1:n.1073_1147del
XR_945790.1:n.1073_1147del
XR_945791.1:n.1073_1147del
NM_000314.7:c.361_435del	NP_000305.3:p.Ala121_Phe145del
NM_001304717.5:c.880_954del	NP_001291646.4:p.Ala294_Phe318del
NM_001304718.2:c.-390_-316del	NP_001291647.1:n.-390_-316del
NM_000314.8:c.361_435del MANE Select	NP_000305.3:p.Ala121_Phe145del