Canonical Allele Identifier: CA891840983

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960897_87960898delinsGC , CM000672.2:g.87960897_87960898delinsGC	GRCh38
NC_000010.10:g.89720654_89720655delinsGC , CM000672.1:g.89720654_89720655delinsGC	GRCh37
NC_000010.9:g.89710634_89710635delinsGC	NCBI36
NG_007466.2:g.102459_102460delinsGC , LRG_311:g.102459_102460delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.898_899delinsGC	ENSP00000514759.2:p.Lys300Ala
ENST00000710265.1:c.805_806delinsGC	ENSP00000518161.1:p.Lys269Ala
ENST00000472832.3:c.805_806delinsGC	ENSP00000483066.2:p.Lys269Ala
ENST00000688158.2:n.1540_1541delinsGC
ENST00000688922.2:c.*635_*636delinsGC	ENSP00000508742.2:n.*635_*636delinsGC
ENST00000700021.1:c.760_761delinsGC	ENSP00000514757.1:p.Lys254Ala
ENST00000700022.1:c.*144_*145delinsGC	ENSP00000514758.1:n.*144_*145delinsGC
ENST00000700023.1:n.1963_1964delinsGC
ENST00000700024.1:n.2197_2198delinsGC
ENST00000700025.1:n.1574_1575delinsGC
ENST00000700026.1:n.442_443delinsGC
ENST00000700029.1:c.732_733delinsGC
ENST00000706954.1:c.805_806delinsGC	ENSP00000516674.1:p.Lys269Ala
ENST00000706955.1:c.*840_*841delinsGC	ENSP00000516675.1:n.*840_*841delinsGC
ENST00000686459.1:c.*391_*392delinsGC	ENSP00000508909.1:n.*391_*392delinsGC
ENST00000688158.1:c.*916_*917delinsGC	ENSP00000509254.1:n.*916_*917delinsGC
ENST00000688308.1:c.805_806delinsGC	ENSP00000508752.1:p.Lys269Ala
ENST00000688922.1:c.726_727delinsGC
ENST00000693560.1:c.1324_1325delinsGC	ENSP00000509861.1:p.Lys442Ala
ENST00000371953.8:c.805_806delinsGC MANE Select	ENSP00000361021.3:p.Lys269Ala
ENST00000371953.7:c.805_806delinsGC	ENSP00000361021.3:p.Lys269Ala
ENST00000472832.2:c.232_233delinsGC	ENSP00000483066.1:p.Lys78Ala
NM_000314.5:c.805_806delinsGC	NP_000305.3:p.Lys269Ala
NM_000314.6:c.805_806delinsGC	NP_000305.3:p.Lys269Ala
NM_001304717.2:c.1324_1325delinsGC	NP_001291646.2:p.Lys442Ala
NM_001304718.1:c.214_215delinsGC	NP_001291647.1:p.Lys72Ala
XM_006717926.2:c.760_761delinsGC	XP_006717989.1:p.Lys254Ala
XM_011539981.1:c.805_806delinsGC	XP_011538283.1:p.Lys269Ala
XM_011539982.1:c.709_710delinsGC	XP_011538284.1:p.Lys237Ala
XR_945791.1:n.1375_1376delinsGC
NM_000314.7:c.805_806delinsGC	NP_000305.3:p.Lys269Ala
NM_001304717.5:c.1324_1325delinsGC	NP_001291646.4:p.Lys442Ala
NM_001304718.2:c.214_215delinsGC	NP_001291647.1:p.Lys72Ala
NM_000314.8:c.805_806delinsGC MANE Select	NP_000305.3:p.Lys269Ala