Canonical Allele Identifier: CA891837416

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965347_87965348delinsCA , CM000672.2:g.87965347_87965348delinsCA	GRCh38
NC_000010.10:g.89725104_89725105delinsCA , CM000672.1:g.89725104_89725105delinsCA	GRCh37
NC_000010.9:g.89715084_89715085delinsCA	NCBI36
NG_007466.2:g.106909_106910delinsCA , LRG_311:g.106909_106910delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1180_1181delinsCA	ENSP00000514759.2:p.Thr394His
ENST00000710265.1:c.*116_*117delinsCA	ENSP00000518161.1:n.*116_*117delinsCA
ENST00000688158.2:n.1822_1823delinsCA
ENST00000688922.2:c.*917_*918delinsCA	ENSP00000508742.2:n.*917_*918delinsCA
ENST00000700021.1:c.1042_1043delinsCA	ENSP00000514757.1:p.Thr348His
ENST00000700022.1:c.*426_*427delinsCA	ENSP00000514758.1:n.*426_*427delinsCA
ENST00000700023.1:n.2245_2246delinsCA
ENST00000700024.1:n.2479_2480delinsCA
ENST00000706954.1:c.1087_1088delinsCA	ENSP00000516674.1:p.Thr363His
ENST00000706955.1:c.*1122_*1123delinsCA	ENSP00000516675.1:n.*1122_*1123delinsCA
ENST00000686459.1:c.*673_*674delinsCA	ENSP00000508909.1:n.*673_*674delinsCA
ENST00000688158.1:c.*1198_*1199delinsCA	ENSP00000509254.1:n.*1198_*1199delinsCA
ENST00000688308.1:c.1087_1088delinsCA	ENSP00000508752.1:p.Thr363His
ENST00000688922.1:c.1008_1009delinsCA
ENST00000693560.1:c.1606_1607delinsCA	ENSP00000509861.1:p.Thr536His
ENST00000371953.8:c.1087_1088delinsCA MANE Select	ENSP00000361021.3:p.Thr363His
ENST00000371953.7:c.1087_1088delinsCA	ENSP00000361021.3:p.Thr363His
NM_000314.5:c.1087_1088delinsCA	NP_000305.3:p.Thr363His
NM_000314.6:c.1087_1088delinsCA	NP_000305.3:p.Thr363His
NM_001304717.2:c.1606_1607delinsCA	NP_001291646.2:p.Thr536His
NM_001304718.1:c.496_497delinsCA	NP_001291647.1:p.Thr166His
XM_006717926.2:c.1042_1043delinsCA	XP_006717989.1:p.Thr348His
XM_011539982.1:c.991_992delinsCA	XP_011538284.1:p.Thr331His
XR_945791.1:n.1657_1658delinsCA
NM_000314.7:c.1087_1088delinsCA	NP_000305.3:p.Thr363His
NM_001304717.5:c.1606_1607delinsCA	NP_001291646.4:p.Thr536His
NM_001304718.2:c.496_497delinsCA	NP_001291647.1:p.Thr166His
NM_000314.8:c.1087_1088delinsCA MANE Select	NP_000305.3:p.Thr363His