Canonical Allele Identifier: CA891839350

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957864_87957866delinsTAT , CM000672.2:g.87957864_87957866delinsTAT	GRCh38
NC_000010.10:g.89717621_89717623delinsTAT , CM000672.1:g.89717621_89717623delinsTAT	GRCh37
NC_000010.9:g.89707601_89707603delinsTAT	NCBI36
NG_007466.2:g.99426_99428delinsTAT , LRG_311:g.99426_99428delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.646_648delinsTAT	ENSP00000514759.2:p.Val216Tyr
ENST00000710265.1:c.646_648delinsTAT	ENSP00000518161.1:p.Val216Tyr
ENST00000472832.3:c.646_648delinsTAT	ENSP00000483066.2:p.Val216Tyr
ENST00000688158.2:n.1381_1383delinsTAT
ENST00000688922.2:c.*476_*478delinsTAT	ENSP00000508742.2:n.*476_*478delinsTAT
ENST00000700021.1:c.601_603delinsTAT	ENSP00000514757.1:p.Val201Tyr
ENST00000700022.1:c.504_506delinsTAT	ENSP00000514758.1:p.Leu168_Trp169delinsPheMet
ENST00000700023.1:n.1804_1806delinsTAT
ENST00000700024.1:n.2038_2040delinsTAT
ENST00000700025.1:n.1415_1417delinsTAT
ENST00000700026.1:n.283_285delinsTAT
ENST00000700029.1:c.480_482delinsTAT
ENST00000706954.1:c.646_648delinsTAT	ENSP00000516674.1:p.Val216Tyr
ENST00000706955.1:c.*681_*683delinsTAT	ENSP00000516675.1:n.*681_*683delinsTAT
ENST00000686459.1:c.*232_*234delinsTAT	ENSP00000508909.1:n.*232_*234delinsTAT
ENST00000688158.1:c.*757_*759delinsTAT	ENSP00000509254.1:n.*757_*759delinsTAT
ENST00000688308.1:c.646_648delinsTAT	ENSP00000508752.1:p.Val216Tyr
ENST00000688922.1:c.567_569delinsTAT
ENST00000693560.1:c.1165_1167delinsTAT	ENSP00000509861.1:p.Val389Tyr
ENST00000371953.8:c.646_648delinsTAT MANE Select	ENSP00000361021.3:p.Val216Tyr
ENST00000371953.7:c.646_648delinsTAT	ENSP00000361021.3:p.Val216Tyr
ENST00000472832.2:c.73_75delinsTAT	ENSP00000483066.1:p.Val25Tyr
NM_000314.5:c.646_648delinsTAT	NP_000305.3:p.Val216Tyr
NM_000314.6:c.646_648delinsTAT	NP_000305.3:p.Val216Tyr
NM_001304717.2:c.1165_1167delinsTAT	NP_001291646.2:p.Val389Tyr
NM_001304718.1:c.55_57delinsTAT	NP_001291647.1:p.Val19Tyr
XM_006717926.2:c.601_603delinsTAT	XP_006717989.1:p.Val201Tyr
XM_011539981.1:c.646_648delinsTAT	XP_011538283.1:p.Val216Tyr
XM_011539982.1:c.550_552delinsTAT	XP_011538284.1:p.Val184Tyr
XR_945791.1:n.1216_1218delinsTAT
NM_000314.7:c.646_648delinsTAT	NP_000305.3:p.Val216Tyr
NM_001304717.5:c.1165_1167delinsTAT	NP_001291646.4:p.Val389Tyr
NM_001304718.2:c.55_57delinsTAT	NP_001291647.1:p.Val19Tyr
NM_000314.8:c.646_648delinsTAT MANE Select	NP_000305.3:p.Val216Tyr