Canonical Allele Identifier: CA891839369

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957867_87957869delinsACT , CM000672.2:g.87957867_87957869delinsACT	GRCh38
NC_000010.10:g.89717624_89717626delinsACT , CM000672.1:g.89717624_89717626delinsACT	GRCh37
NC_000010.9:g.89707604_89707606delinsACT	NCBI36
NG_007466.2:g.99429_99431delinsACT , LRG_311:g.99429_99431delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.649_651delinsACT	ENSP00000514759.2:p.Val217Thr
ENST00000710265.1:c.649_651delinsACT	ENSP00000518161.1:p.Val217Thr
ENST00000472832.3:c.649_651delinsACT	ENSP00000483066.2:p.Val217Thr
ENST00000688158.2:n.1384_1386delinsACT
ENST00000688922.2:c.*479_*481delinsACT	ENSP00000508742.2:n.*479_*481delinsACT
ENST00000700021.1:c.604_606delinsACT	ENSP00000514757.1:p.Val202Thr
ENST00000700022.1:c.507_509delinsACT	ENSP00000514758.1:p.Trp169Ter
ENST00000700023.1:n.1807_1809delinsACT
ENST00000700024.1:n.2041_2043delinsACT
ENST00000700025.1:n.1418_1420delinsACT
ENST00000700026.1:n.286_288delinsACT
ENST00000700029.1:c.483_485delinsACT
ENST00000706954.1:c.649_651delinsACT	ENSP00000516674.1:p.Val217Thr
ENST00000706955.1:c.*684_*686delinsACT	ENSP00000516675.1:n.*684_*686delinsACT
ENST00000686459.1:c.*235_*237delinsACT	ENSP00000508909.1:n.*235_*237delinsACT
ENST00000688158.1:c.*760_*762delinsACT	ENSP00000509254.1:n.*760_*762delinsACT
ENST00000688308.1:c.649_651delinsACT	ENSP00000508752.1:p.Val217Thr
ENST00000688922.1:c.570_572delinsACT
ENST00000693560.1:c.1168_1170delinsACT	ENSP00000509861.1:p.Val390Thr
ENST00000371953.8:c.649_651delinsACT MANE Select	ENSP00000361021.3:p.Val217Thr
ENST00000371953.7:c.649_651delinsACT	ENSP00000361021.3:p.Val217Thr
ENST00000472832.2:c.76_78delinsACT	ENSP00000483066.1:p.Val26Thr
NM_000314.5:c.649_651delinsACT	NP_000305.3:p.Val217Thr
NM_000314.6:c.649_651delinsACT	NP_000305.3:p.Val217Thr
NM_001304717.2:c.1168_1170delinsACT	NP_001291646.2:p.Val390Thr
NM_001304718.1:c.58_60delinsACT	NP_001291647.1:p.Val20Thr
XM_006717926.2:c.604_606delinsACT	XP_006717989.1:p.Val202Thr
XM_011539981.1:c.649_651delinsACT	XP_011538283.1:p.Val217Thr
XM_011539982.1:c.553_555delinsACT	XP_011538284.1:p.Val185Thr
XR_945791.1:n.1219_1221delinsACT
NM_000314.7:c.649_651delinsACT	NP_000305.3:p.Val217Thr
NM_001304717.5:c.1168_1170delinsACT	NP_001291646.4:p.Val390Thr
NM_001304718.2:c.58_60delinsACT	NP_001291647.1:p.Val20Thr
NM_000314.8:c.649_651delinsACT MANE Select	NP_000305.3:p.Val217Thr