Canonical Allele Identifier: CA891841291

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952148_87952149delinsCG , CM000672.2:g.87952148_87952149delinsCG	GRCh38
NC_000010.10:g.89711905_89711906delinsCG , CM000672.1:g.89711905_89711906delinsCG	GRCh37
NC_000010.9:g.89701885_89701886delinsCG	NCBI36
NG_007466.2:g.93710_93711delinsCG , LRG_311:g.93710_93711delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.523_524delinsCG	ENSP00000514759.2:p.Val175Arg
ENST00000710265.1:c.523_524delinsCG	ENSP00000518161.1:p.Val175Arg
ENST00000472832.3:c.523_524delinsCG	ENSP00000483066.2:p.Val175Arg
ENST00000688158.2:n.1258_1259delinsCG
ENST00000688922.2:c.*353_*354delinsCG	ENSP00000508742.2:n.*353_*354delinsCG
ENST00000700021.1:c.478_479delinsCG	ENSP00000514757.1:p.Val160Arg
ENST00000700022.1:c.493-5705_493-5704delinsCG	ENSP00000514758.1:n.493-5705_493-5704deli...
ENST00000700023.1:n.1681_1682delinsCG
ENST00000700024.1:n.1915_1916delinsCG
ENST00000700025.1:n.1292_1293delinsCG
ENST00000700029.1:c.357_358delinsCG
ENST00000706954.1:c.523_524delinsCG	ENSP00000516674.1:p.Val175Arg
ENST00000706955.1:c.*558_*559delinsCG	ENSP00000516675.1:n.*558_*559delinsCG
ENST00000686459.1:c.*109_*110delinsCG	ENSP00000508909.1:n.*109_*110delinsCG
ENST00000688158.1:c.*634_*635delinsCG	ENSP00000509254.1:n.*634_*635delinsCG
ENST00000688308.1:c.523_524delinsCG	ENSP00000508752.1:p.Val175Arg
ENST00000688922.1:c.444_445delinsCG
ENST00000693560.1:c.1042_1043delinsCG	ENSP00000509861.1:p.Val348Arg
ENST00000371953.8:c.523_524delinsCG MANE Select	ENSP00000361021.3:p.Val175Arg
ENST00000371953.7:c.523_524delinsCG	ENSP00000361021.3:p.Val175Arg
NM_000314.5:c.523_524delinsCG	NP_000305.3:p.Val175Arg
NM_000314.6:c.523_524delinsCG	NP_000305.3:p.Val175Arg
NM_001304717.2:c.1042_1043delinsCG	NP_001291646.2:p.Val348Arg
NM_001304718.1:c.-69_-68delinsCG	NP_001291647.1:n.-69_-68delinsCG
XM_006717926.2:c.478_479delinsCG	XP_006717989.1:p.Val160Arg
XM_011539981.1:c.523_524delinsCG	XP_011538283.1:p.Val175Arg
XM_011539982.1:c.427_428delinsCG	XP_011538284.1:p.Val143Arg
XR_945789.1:n.1394_1395delinsCG
XR_945790.1:n.1511_1512delinsCG
XR_945791.1:n.1205-5705_1205-5704delinsCG
NM_000314.7:c.523_524delinsCG	NP_000305.3:p.Val175Arg
NM_001304717.5:c.1042_1043delinsCG	NP_001291646.4:p.Val348Arg
NM_001304718.2:c.-69_-68delinsCG	NP_001291647.1:n.-69_-68delinsCG
NM_000314.8:c.523_524delinsCG MANE Select	NP_000305.3:p.Val175Arg