Canonical Allele Identifier: CA891835093

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925544_87925546delinsTCT , CM000672.2:g.87925544_87925546delinsTCT	GRCh38
NC_000010.10:g.89685301_89685303delinsTCT , CM000672.1:g.89685301_89685303delinsTCT	GRCh37
NC_000010.9:g.89675281_89675283delinsTCT	NCBI36
NG_007466.2:g.67106_67108delinsTCT , LRG_311:g.67106_67108delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.196_198delinsTCT	ENSP00000514759.2:p.Lys66Ser
ENST00000710265.1:c.196_198delinsTCT	ENSP00000518161.1:p.Lys66Ser
ENST00000472832.3:c.196_198delinsTCT	ENSP00000483066.2:p.Lys66Ser
ENST00000688158.2:n.931_933delinsTCT
ENST00000688922.2:c.196_198delinsTCT	ENSP00000508742.2:p.Lys66Ser
ENST00000700021.1:c.165-5502_165-5500delinsTCT	ENSP00000514757.1:n.165-5502_165-5500delinsTCT
ENST00000700022.1:c.196_198delinsTCT	ENSP00000514758.1:p.Lys66Ser
ENST00000700029.1:c.30_32delinsTCT
ENST00000706954.1:c.196_198delinsTCT	ENSP00000516674.1:p.Lys66Ser
ENST00000706955.1:c.*231_*233delinsTCT	ENSP00000516675.1:n.*231_*233delinsTCT
ENST00000686459.1:c.196_198delinsTCT	ENSP00000508909.1:p.Lys66Ser
ENST00000688158.1:c.*307_*309delinsTCT	ENSP00000509254.1:n.*307_*309delinsTCT
ENST00000688308.1:c.196_198delinsTCT	ENSP00000508752.1:p.Lys66Ser
ENST00000688922.1:c.65_67delinsTCT
ENST00000693560.1:c.715_717delinsTCT	ENSP00000509861.1:p.Lys239Ser
ENST00000371953.8:c.196_198delinsTCT MANE Select	ENSP00000361021.3:p.Lys66Ser
ENST00000371953.7:c.196_198delinsTCT	ENSP00000361021.3:p.Lys66Ser
ENST00000498703.1:n.22_24delinsTCT
ENST00000610634.1:c.94_96delinsTCT	ENSP00000477517.1:p.Lys32Ser
NM_000314.5:c.196_198delinsTCT	NP_000305.3:p.Lys66Ser
NM_000314.6:c.196_198delinsTCT	NP_000305.3:p.Lys66Ser
NM_001304717.2:c.715_717delinsTCT	NP_001291646.2:p.Lys239Ser
NM_001304718.1:c.-541-5502_-541-5500delinsTCT	NP_001291647.1:n.-541-5502_-541-5500delinsTCT
XM_006717926.2:c.165-5502_165-5500delinsTCT	XP_006717989.1:n.165-5502_165-5500delinsTCT
XM_011539981.1:c.196_198delinsTCT	XP_011538283.1:p.Lys66Ser
XM_011539982.1:c.100_102delinsTCT	XP_011538284.1:p.Lys34Ser
XR_945789.1:n.908_910delinsTCT
XR_945790.1:n.908_910delinsTCT
XR_945791.1:n.908_910delinsTCT
NM_000314.7:c.196_198delinsTCT	NP_000305.3:p.Lys66Ser
NM_001304717.5:c.715_717delinsTCT	NP_001291646.4:p.Lys239Ser
NM_001304718.2:c.-541-5502_-541-5500delinsTCT	NP_001291647.1:n.-541-5502_-541-5500delinsTCT
NM_000314.8:c.196_198delinsTCT MANE Select	NP_000305.3:p.Lys66Ser