Canonical Allele Identifier: CA891841294

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961048_87961049delinsAA , CM000672.2:g.87961048_87961049delinsAA	GRCh38
NC_000010.10:g.89720805_89720806delinsAA , CM000672.1:g.89720805_89720806delinsAA	GRCh37
NC_000010.9:g.89710785_89710786delinsAA	NCBI36
NG_007466.2:g.102610_102611delinsAA , LRG_311:g.102610_102611delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1049_1050delinsAA	ENSP00000514759.2:p.Thr350Lys
ENST00000710265.1:c.956_957delinsAA	ENSP00000518161.1:p.Thr319Lys
ENST00000472832.3:c.956_957delinsAA	ENSP00000483066.2:p.Thr319Lys
ENST00000688158.2:n.1691_1692delinsAA
ENST00000688922.2:c.*786_*787delinsAA	ENSP00000508742.2:n.*786_*787delinsAA
ENST00000700021.1:c.911_912delinsAA	ENSP00000514757.1:p.Thr304Lys
ENST00000700022.1:c.*295_*296delinsAA	ENSP00000514758.1:n.*295_*296delinsAA
ENST00000700023.1:n.2114_2115delinsAA
ENST00000700024.1:n.2348_2349delinsAA
ENST00000700025.1:n.1725_1726delinsAA
ENST00000700026.1:n.593_594delinsAA
ENST00000706954.1:c.956_957delinsAA	ENSP00000516674.1:p.Thr319Lys
ENST00000706955.1:c.*991_*992delinsAA	ENSP00000516675.1:n.*991_*992delinsAA
ENST00000686459.1:c.*542_*543delinsAA	ENSP00000508909.1:n.*542_*543delinsAA
ENST00000688158.1:c.*1067_*1068delinsAA	ENSP00000509254.1:n.*1067_*1068delinsAA
ENST00000688308.1:c.956_957delinsAA	ENSP00000508752.1:p.Thr319Lys
ENST00000688922.1:c.877_878delinsAA
ENST00000693560.1:c.1475_1476delinsAA	ENSP00000509861.1:p.Thr492Lys
ENST00000371953.8:c.956_957delinsAA MANE Select	ENSP00000361021.3:p.Thr319Lys
ENST00000371953.7:c.956_957delinsAA	ENSP00000361021.3:p.Thr319Lys
ENST00000472832.2:c.383_384delinsAA	ENSP00000483066.1:p.Thr128Lys
NM_000314.5:c.956_957delinsAA	NP_000305.3:p.Thr319Lys
NM_000314.6:c.956_957delinsAA	NP_000305.3:p.Thr319Lys
NM_001304717.2:c.1475_1476delinsAA	NP_001291646.2:p.Thr492Lys
NM_001304718.1:c.365_366delinsAA	NP_001291647.1:p.Thr122Lys
XM_006717926.2:c.911_912delinsAA	XP_006717989.1:p.Thr304Lys
XM_011539981.1:c.956_957delinsAA	XP_011538283.1:p.Thr319Lys
XM_011539982.1:c.860_861delinsAA	XP_011538284.1:p.Thr287Lys
XR_945791.1:n.1526_1527delinsAA
NM_000314.7:c.956_957delinsAA	NP_000305.3:p.Thr319Lys
NM_001304717.5:c.1475_1476delinsAA	NP_001291646.4:p.Thr492Lys
NM_001304718.2:c.365_366delinsAA	NP_001291647.1:p.Thr122Lys
NM_000314.8:c.956_957delinsAA MANE Select	NP_000305.3:p.Thr319Lys