Canonical Allele Identifier: CA891838870

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952170_87952171delinsCT , CM000672.2:g.87952170_87952171delinsCT	GRCh38
NC_000010.10:g.89711927_89711928delinsCT , CM000672.1:g.89711927_89711928delinsCT	GRCh37
NC_000010.9:g.89701907_89701908delinsCT	NCBI36
NG_007466.2:g.93732_93733delinsCT , LRG_311:g.93732_93733delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.545_546delinsCT	ENSP00000514759.2:p.Leu182Ser
ENST00000710265.1:c.545_546delinsCT	ENSP00000518161.1:p.Leu182Ser
ENST00000472832.3:c.545_546delinsCT	ENSP00000483066.2:p.Leu182Ser
ENST00000688158.2:n.1280_1281delinsCT
ENST00000688922.2:c.*375_*376delinsCT	ENSP00000508742.2:n.*375_*376delinsCT
ENST00000700021.1:c.500_501delinsCT	ENSP00000514757.1:p.Leu167Ser
ENST00000700022.1:c.493-5683_493-5682delinsCT	ENSP00000514758.1:n.493-5683_493-5682delinsCT
ENST00000700023.1:n.1703_1704delinsCT
ENST00000700024.1:n.1937_1938delinsCT
ENST00000700025.1:n.1314_1315delinsCT
ENST00000700029.1:c.379_380delinsCT
ENST00000706954.1:c.545_546delinsCT	ENSP00000516674.1:p.Leu182Ser
ENST00000706955.1:c.*580_*581delinsCT	ENSP00000516675.1:n.*580_*581delinsCT
ENST00000686459.1:c.*131_*132delinsCT	ENSP00000508909.1:n.*131_*132delinsCT
ENST00000688158.1:c.*656_*657delinsCT	ENSP00000509254.1:n.*656_*657delinsCT
ENST00000688308.1:c.545_546delinsCT	ENSP00000508752.1:p.Leu182Ser
ENST00000688922.1:c.466_467delinsCT
ENST00000693560.1:c.1064_1065delinsCT	ENSP00000509861.1:p.Leu355Ser
ENST00000371953.8:c.545_546delinsCT MANE Select	ENSP00000361021.3:p.Leu182Ser
ENST00000371953.7:c.545_546delinsCT	ENSP00000361021.3:p.Leu182Ser
NM_000314.5:c.545_546delinsCT	NP_000305.3:p.Leu182Ser
NM_000314.6:c.545_546delinsCT	NP_000305.3:p.Leu182Ser
NM_001304717.2:c.1064_1065delinsCT	NP_001291646.2:p.Leu355Ser
NM_001304718.1:c.-47_-46delinsCT	NP_001291647.1:n.-47_-46delinsCT
XM_006717926.2:c.500_501delinsCT	XP_006717989.1:p.Leu167Ser
XM_011539981.1:c.545_546delinsCT	XP_011538283.1:p.Leu182Ser
XM_011539982.1:c.449_450delinsCT	XP_011538284.1:p.Leu150Ser
XR_945789.1:n.1416_1417delinsCT
XR_945790.1:n.1533_1534delinsCT
XR_945791.1:n.1205-5683_1205-5682delinsCT
NM_000314.7:c.545_546delinsCT	NP_000305.3:p.Leu182Ser
NM_001304717.5:c.1064_1065delinsCT	NP_001291646.4:p.Leu355Ser
NM_001304718.2:c.-47_-46delinsCT	NP_001291647.1:n.-47_-46delinsCT
NM_000314.8:c.545_546delinsCT MANE Select	NP_000305.3:p.Leu182Ser