Canonical Allele Identifier: CA891840342

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957861_87957862delinsCC , CM000672.2:g.87957861_87957862delinsCC	GRCh38
NC_000010.10:g.89717618_89717619delinsCC , CM000672.1:g.89717618_89717619delinsCC	GRCh37
NC_000010.9:g.89707598_89707599delinsCC	NCBI36
NG_007466.2:g.99423_99424delinsCC , LRG_311:g.99423_99424delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.643_644delinsCC	ENSP00000514759.2:p.Phe215Pro
ENST00000710265.1:c.643_644delinsCC	ENSP00000518161.1:p.Phe215Pro
ENST00000472832.3:c.643_644delinsCC	ENSP00000483066.2:p.Phe215Pro
ENST00000688158.2:n.1378_1379delinsCC
ENST00000688922.2:c.*473_*474delinsCC	ENSP00000508742.2:n.*473_*474delinsCC
ENST00000700021.1:c.598_599delinsCC	ENSP00000514757.1:p.Phe200Pro
ENST00000700022.1:c.501_502delinsCC	ENSP00000514758.1:p.Ser167=
ENST00000700023.1:n.1801_1802delinsCC
ENST00000700024.1:n.2035_2036delinsCC
ENST00000700025.1:n.1412_1413delinsCC
ENST00000700026.1:n.280_281delinsCC
ENST00000700029.1:c.477_478delinsCC
ENST00000706954.1:c.643_644delinsCC	ENSP00000516674.1:p.Phe215Pro
ENST00000706955.1:c.*678_*679delinsCC	ENSP00000516675.1:n.*678_*679delinsCC
ENST00000686459.1:c.*229_*230delinsCC	ENSP00000508909.1:n.*229_*230delinsCC
ENST00000688158.1:c.*754_*755delinsCC	ENSP00000509254.1:n.*754_*755delinsCC
ENST00000688308.1:c.643_644delinsCC	ENSP00000508752.1:p.Phe215Pro
ENST00000688922.1:c.564_565delinsCC
ENST00000693560.1:c.1162_1163delinsCC	ENSP00000509861.1:p.Phe388Pro
ENST00000371953.8:c.643_644delinsCC MANE Select	ENSP00000361021.3:p.Phe215Pro
ENST00000371953.7:c.643_644delinsCC	ENSP00000361021.3:p.Phe215Pro
ENST00000472832.2:c.70_71delinsCC	ENSP00000483066.1:p.Phe24Pro
NM_000314.5:c.643_644delinsCC	NP_000305.3:p.Phe215Pro
NM_000314.6:c.643_644delinsCC	NP_000305.3:p.Phe215Pro
NM_001304717.2:c.1162_1163delinsCC	NP_001291646.2:p.Phe388Pro
NM_001304718.1:c.52_53delinsCC	NP_001291647.1:p.Phe18Pro
XM_006717926.2:c.598_599delinsCC	XP_006717989.1:p.Phe200Pro
XM_011539981.1:c.643_644delinsCC	XP_011538283.1:p.Phe215Pro
XM_011539982.1:c.547_548delinsCC	XP_011538284.1:p.Phe183Pro
XR_945791.1:n.1213_1214delinsCC
NM_000314.7:c.643_644delinsCC	NP_000305.3:p.Phe215Pro
NM_001304717.5:c.1162_1163delinsCC	NP_001291646.4:p.Phe388Pro
NM_001304718.2:c.52_53delinsCC	NP_001291647.1:p.Phe18Pro
NM_000314.8:c.643_644delinsCC MANE Select	NP_000305.3:p.Phe215Pro