Canonical Allele Identifier: CA891836551

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961048_87961049delinsGA , CM000672.2:g.87961048_87961049delinsGA	GRCh38
NC_000010.10:g.89720805_89720806delinsGA , CM000672.1:g.89720805_89720806delinsGA	GRCh37
NC_000010.9:g.89710785_89710786delinsGA	NCBI36
NG_007466.2:g.102610_102611delinsGA , LRG_311:g.102610_102611delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1049_1050delinsGA	ENSP00000514759.2:p.Thr350Arg
ENST00000710265.1:c.956_957delinsGA	ENSP00000518161.1:p.Thr319Arg
ENST00000472832.3:c.956_957delinsGA	ENSP00000483066.2:p.Thr319Arg
ENST00000688158.2:n.1691_1692delinsGA
ENST00000688922.2:c.*786_*787delinsGA	ENSP00000508742.2:n.*786_*787delinsGA
ENST00000700021.1:c.911_912delinsGA	ENSP00000514757.1:p.Thr304Arg
ENST00000700022.1:c.*295_*296delinsGA	ENSP00000514758.1:n.*295_*296delinsGA
ENST00000700023.1:n.2114_2115delinsGA
ENST00000700024.1:n.2348_2349delinsGA
ENST00000700025.1:n.1725_1726delinsGA
ENST00000700026.1:n.593_594delinsGA
ENST00000706954.1:c.956_957delinsGA	ENSP00000516674.1:p.Thr319Arg
ENST00000706955.1:c.*991_*992delinsGA	ENSP00000516675.1:n.*991_*992delinsGA
ENST00000686459.1:c.*542_*543delinsGA	ENSP00000508909.1:n.*542_*543delinsGA
ENST00000688158.1:c.*1067_*1068delinsGA	ENSP00000509254.1:n.*1067_*1068delinsGA
ENST00000688308.1:c.956_957delinsGA	ENSP00000508752.1:p.Thr319Arg
ENST00000688922.1:c.877_878delinsGA
ENST00000693560.1:c.1475_1476delinsGA	ENSP00000509861.1:p.Thr492Arg
ENST00000371953.8:c.956_957delinsGA MANE Select	ENSP00000361021.3:p.Thr319Arg
ENST00000371953.7:c.956_957delinsGA	ENSP00000361021.3:p.Thr319Arg
ENST00000472832.2:c.383_384delinsGA	ENSP00000483066.1:p.Thr128Arg
NM_000314.5:c.956_957delinsGA	NP_000305.3:p.Thr319Arg
NM_000314.6:c.956_957delinsGA	NP_000305.3:p.Thr319Arg
NM_001304717.2:c.1475_1476delinsGA	NP_001291646.2:p.Thr492Arg
NM_001304718.1:c.365_366delinsGA	NP_001291647.1:p.Thr122Arg
XM_006717926.2:c.911_912delinsGA	XP_006717989.1:p.Thr304Arg
XM_011539981.1:c.956_957delinsGA	XP_011538283.1:p.Thr319Arg
XM_011539982.1:c.860_861delinsGA	XP_011538284.1:p.Thr287Arg
XR_945791.1:n.1526_1527delinsGA
NM_000314.7:c.956_957delinsGA	NP_000305.3:p.Thr319Arg
NM_001304717.5:c.1475_1476delinsGA	NP_001291646.4:p.Thr492Arg
NM_001304718.2:c.365_366delinsGA	NP_001291647.1:p.Thr122Arg
NM_000314.8:c.956_957delinsGA MANE Select	NP_000305.3:p.Thr319Arg