Canonical Allele Identifier: CA891838779

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952151_87952152delinsGT , CM000672.2:g.87952151_87952152delinsGT	GRCh38
NC_000010.10:g.89711908_89711909delinsGT , CM000672.1:g.89711908_89711909delinsGT	GRCh37
NC_000010.9:g.89701888_89701889delinsGT	NCBI36
NG_007466.2:g.93713_93714delinsGT , LRG_311:g.93713_93714delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.526_527delinsGT	ENSP00000514759.2:p.Tyr176Val
ENST00000710265.1:c.526_527delinsGT	ENSP00000518161.1:p.Tyr176Val
ENST00000472832.3:c.526_527delinsGT	ENSP00000483066.2:p.Tyr176Val
ENST00000688158.2:n.1261_1262delinsGT
ENST00000688922.2:c.*356_*357delinsGT	ENSP00000508742.2:n.*356_*357delinsGT
ENST00000700021.1:c.481_482delinsGT	ENSP00000514757.1:p.Tyr161Val
ENST00000700022.1:c.493-5702_493-5701delinsGT	ENSP00000514758.1:n.493-5702_493-5701delinsGT
ENST00000700023.1:n.1684_1685delinsGT
ENST00000700024.1:n.1918_1919delinsGT
ENST00000700025.1:n.1295_1296delinsGT
ENST00000700029.1:c.360_361delinsGT
ENST00000706954.1:c.526_527delinsGT	ENSP00000516674.1:p.Tyr176Val
ENST00000706955.1:c.*561_*562delinsGT	ENSP00000516675.1:n.*561_*562delinsGT
ENST00000686459.1:c.*112_*113delinsGT	ENSP00000508909.1:n.*112_*113delinsGT
ENST00000688158.1:c.*637_*638delinsGT	ENSP00000509254.1:n.*637_*638delinsGT
ENST00000688308.1:c.526_527delinsGT	ENSP00000508752.1:p.Tyr176Val
ENST00000688922.1:c.447_448delinsGT
ENST00000693560.1:c.1045_1046delinsGT	ENSP00000509861.1:p.Tyr349Val
ENST00000371953.8:c.526_527delinsGT MANE Select	ENSP00000361021.3:p.Tyr176Val
ENST00000371953.7:c.526_527delinsGT	ENSP00000361021.3:p.Tyr176Val
NM_000314.5:c.526_527delinsGT	NP_000305.3:p.Tyr176Val
NM_000314.6:c.526_527delinsGT	NP_000305.3:p.Tyr176Val
NM_001304717.2:c.1045_1046delinsGT	NP_001291646.2:p.Tyr349Val
NM_001304718.1:c.-66_-65delinsGT	NP_001291647.1:n.-66_-65delinsGT
XM_006717926.2:c.481_482delinsGT	XP_006717989.1:p.Tyr161Val
XM_011539981.1:c.526_527delinsGT	XP_011538283.1:p.Tyr176Val
XM_011539982.1:c.430_431delinsGT	XP_011538284.1:p.Tyr144Val
XR_945789.1:n.1397_1398delinsGT
XR_945790.1:n.1514_1515delinsGT
XR_945791.1:n.1205-5702_1205-5701delinsGT
NM_000314.7:c.526_527delinsGT	NP_000305.3:p.Tyr176Val
NM_001304717.5:c.1045_1046delinsGT	NP_001291646.4:p.Tyr349Val
NM_001304718.2:c.-66_-65delinsGT	NP_001291647.1:n.-66_-65delinsGT
NM_000314.8:c.526_527delinsGT MANE Select	NP_000305.3:p.Tyr176Val