Canonical Allele Identifier: CA891840362

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957864_87957866delinsATT , CM000672.2:g.87957864_87957866delinsATT	GRCh38
NC_000010.10:g.89717621_89717623delinsATT , CM000672.1:g.89717621_89717623delinsATT	GRCh37
NC_000010.9:g.89707601_89707603delinsATT	NCBI36
NG_007466.2:g.99426_99428delinsATT , LRG_311:g.99426_99428delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.646_648delinsATT	ENSP00000514759.2:p.Val216Ile
ENST00000710265.1:c.646_648delinsATT	ENSP00000518161.1:p.Val216Ile
ENST00000472832.3:c.646_648delinsATT	ENSP00000483066.2:p.Val216Ile
ENST00000688158.2:n.1381_1383delinsATT
ENST00000688922.2:c.*476_*478delinsATT	ENSP00000508742.2:n.*476_*478delinsATT
ENST00000700021.1:c.601_603delinsATT	ENSP00000514757.1:p.Val201Ile
ENST00000700022.1:c.504_506delinsATT	ENSP00000514758.1:p.Trp169Leu
ENST00000700023.1:n.1804_1806delinsATT
ENST00000700024.1:n.2038_2040delinsATT
ENST00000700025.1:n.1415_1417delinsATT
ENST00000700026.1:n.283_285delinsATT
ENST00000700029.1:c.480_482delinsATT
ENST00000706954.1:c.646_648delinsATT	ENSP00000516674.1:p.Val216Ile
ENST00000706955.1:c.*681_*683delinsATT	ENSP00000516675.1:n.*681_*683delinsATT
ENST00000686459.1:c.*232_*234delinsATT	ENSP00000508909.1:n.*232_*234delinsATT
ENST00000688158.1:c.*757_*759delinsATT	ENSP00000509254.1:n.*757_*759delinsATT
ENST00000688308.1:c.646_648delinsATT	ENSP00000508752.1:p.Val216Ile
ENST00000688922.1:c.567_569delinsATT
ENST00000693560.1:c.1165_1167delinsATT	ENSP00000509861.1:p.Val389Ile
ENST00000371953.8:c.646_648delinsATT MANE Select	ENSP00000361021.3:p.Val216Ile
ENST00000371953.7:c.646_648delinsATT	ENSP00000361021.3:p.Val216Ile
ENST00000472832.2:c.73_75delinsATT	ENSP00000483066.1:p.Val25Ile
NM_000314.5:c.646_648delinsATT	NP_000305.3:p.Val216Ile
NM_000314.6:c.646_648delinsATT	NP_000305.3:p.Val216Ile
NM_001304717.2:c.1165_1167delinsATT	NP_001291646.2:p.Val389Ile
NM_001304718.1:c.55_57delinsATT	NP_001291647.1:p.Val19Ile
XM_006717926.2:c.601_603delinsATT	XP_006717989.1:p.Val201Ile
XM_011539981.1:c.646_648delinsATT	XP_011538283.1:p.Val216Ile
XM_011539982.1:c.550_552delinsATT	XP_011538284.1:p.Val184Ile
XR_945791.1:n.1216_1218delinsATT
NM_000314.7:c.646_648delinsATT	NP_000305.3:p.Val216Ile
NM_001304717.5:c.1165_1167delinsATT	NP_001291646.4:p.Val389Ile
NM_001304718.2:c.55_57delinsATT	NP_001291647.1:p.Val19Ile
NM_000314.8:c.646_648delinsATT MANE Select	NP_000305.3:p.Val216Ile