Canonical Allele Identifier: CA891840456

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957882_87957883delinsTA , CM000672.2:g.87957882_87957883delinsTA	GRCh38
NC_000010.10:g.89717639_89717640delinsTA , CM000672.1:g.89717639_89717640delinsTA	GRCh37
NC_000010.9:g.89707619_89707620delinsTA	NCBI36
NG_007466.2:g.99444_99445delinsTA , LRG_311:g.99444_99445delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.664_665delinsTA	ENSP00000514759.2:p.Val222Ter
ENST00000710265.1:c.664_665delinsTA	ENSP00000518161.1:p.Val222Ter
ENST00000472832.3:c.664_665delinsTA	ENSP00000483066.2:p.Val222Ter
ENST00000688158.2:n.1399_1400delinsTA
ENST00000688922.2:c.*494_*495delinsTA	ENSP00000508742.2:n.*494_*495delinsTA
ENST00000700021.1:c.619_620delinsTA	ENSP00000514757.1:p.Val207Ter
ENST00000700022.1:c.*3_*4delinsTA	ENSP00000514758.1:n.*3_*4delinsTA
ENST00000700023.1:n.1822_1823delinsTA
ENST00000700024.1:n.2056_2057delinsTA
ENST00000700025.1:n.1433_1434delinsTA
ENST00000700026.1:n.301_302delinsTA
ENST00000700029.1:c.498_499delinsTA
ENST00000706954.1:c.664_665delinsTA	ENSP00000516674.1:p.Val222Ter
ENST00000706955.1:c.*699_*700delinsTA	ENSP00000516675.1:n.*699_*700delinsTA
ENST00000686459.1:c.*250_*251delinsTA	ENSP00000508909.1:n.*250_*251delinsTA
ENST00000688158.1:c.*775_*776delinsTA	ENSP00000509254.1:n.*775_*776delinsTA
ENST00000688308.1:c.664_665delinsTA	ENSP00000508752.1:p.Val222Ter
ENST00000688922.1:c.585_586delinsTA
ENST00000693560.1:c.1183_1184delinsTA	ENSP00000509861.1:p.Val395Ter
ENST00000371953.8:c.664_665delinsTA MANE Select	ENSP00000361021.3:p.Val222Ter
ENST00000371953.7:c.664_665delinsTA	ENSP00000361021.3:p.Val222Ter
ENST00000472832.2:c.91_92delinsTA	ENSP00000483066.1:p.Val31Ter
NM_000314.5:c.664_665delinsTA	NP_000305.3:p.Val222Ter
NM_000314.6:c.664_665delinsTA	NP_000305.3:p.Val222Ter
NM_001304717.2:c.1183_1184delinsTA	NP_001291646.2:p.Val395Ter
NM_001304718.1:c.73_74delinsTA	NP_001291647.1:p.Val25Ter
XM_006717926.2:c.619_620delinsTA	XP_006717989.1:p.Val207Ter
XM_011539981.1:c.664_665delinsTA	XP_011538283.1:p.Val222Ter
XM_011539982.1:c.568_569delinsTA	XP_011538284.1:p.Val190Ter
XR_945791.1:n.1234_1235delinsTA
NM_000314.7:c.664_665delinsTA	NP_000305.3:p.Val222Ter
NM_001304717.5:c.1183_1184delinsTA	NP_001291646.4:p.Val395Ter
NM_001304718.2:c.73_74delinsTA	NP_001291647.1:p.Val25Ter
NM_000314.8:c.664_665delinsTA MANE Select	NP_000305.3:p.Val222Ter