Canonical Allele Identifier: CA891840978

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960897_87960898delinsGT , CM000672.2:g.87960897_87960898delinsGT	GRCh38
NC_000010.10:g.89720654_89720655delinsGT , CM000672.1:g.89720654_89720655delinsGT	GRCh37
NC_000010.9:g.89710634_89710635delinsGT	NCBI36
NG_007466.2:g.102459_102460delinsGT , LRG_311:g.102459_102460delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.898_899delinsGT	ENSP00000514759.2:p.Lys300Val
ENST00000710265.1:c.805_806delinsGT	ENSP00000518161.1:p.Lys269Val
ENST00000472832.3:c.805_806delinsGT	ENSP00000483066.2:p.Lys269Val
ENST00000688158.2:n.1540_1541delinsGT
ENST00000688922.2:c.*635_*636delinsGT	ENSP00000508742.2:n.*635_*636delinsGT
ENST00000700021.1:c.760_761delinsGT	ENSP00000514757.1:p.Lys254Val
ENST00000700022.1:c.*144_*145delinsGT	ENSP00000514758.1:n.*144_*145delinsGT
ENST00000700023.1:n.1963_1964delinsGT
ENST00000700024.1:n.2197_2198delinsGT
ENST00000700025.1:n.1574_1575delinsGT
ENST00000700026.1:n.442_443delinsGT
ENST00000700029.1:c.732_733delinsGT
ENST00000706954.1:c.805_806delinsGT	ENSP00000516674.1:p.Lys269Val
ENST00000706955.1:c.*840_*841delinsGT	ENSP00000516675.1:n.*840_*841delinsGT
ENST00000686459.1:c.*391_*392delinsGT	ENSP00000508909.1:n.*391_*392delinsGT
ENST00000688158.1:c.*916_*917delinsGT	ENSP00000509254.1:n.*916_*917delinsGT
ENST00000688308.1:c.805_806delinsGT	ENSP00000508752.1:p.Lys269Val
ENST00000688922.1:c.726_727delinsGT
ENST00000693560.1:c.1324_1325delinsGT	ENSP00000509861.1:p.Lys442Val
ENST00000371953.8:c.805_806delinsGT MANE Select	ENSP00000361021.3:p.Lys269Val
ENST00000371953.7:c.805_806delinsGT	ENSP00000361021.3:p.Lys269Val
ENST00000472832.2:c.232_233delinsGT	ENSP00000483066.1:p.Lys78Val
NM_000314.5:c.805_806delinsGT	NP_000305.3:p.Lys269Val
NM_000314.6:c.805_806delinsGT	NP_000305.3:p.Lys269Val
NM_001304717.2:c.1324_1325delinsGT	NP_001291646.2:p.Lys442Val
NM_001304718.1:c.214_215delinsGT	NP_001291647.1:p.Lys72Val
XM_006717926.2:c.760_761delinsGT	XP_006717989.1:p.Lys254Val
XM_011539981.1:c.805_806delinsGT	XP_011538283.1:p.Lys269Val
XM_011539982.1:c.709_710delinsGT	XP_011538284.1:p.Lys237Val
XR_945791.1:n.1375_1376delinsGT
NM_000314.7:c.805_806delinsGT	NP_000305.3:p.Lys269Val
NM_001304717.5:c.1324_1325delinsGT	NP_001291646.4:p.Lys442Val
NM_001304718.2:c.214_215delinsGT	NP_001291647.1:p.Lys72Val
NM_000314.8:c.805_806delinsGT MANE Select	NP_000305.3:p.Lys269Val