Canonical Allele Identifier: CA891836321

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961029_87961031delinsTCT , CM000672.2:g.87961029_87961031delinsTCT	GRCh38
NC_000010.10:g.89720786_89720788delinsTCT , CM000672.1:g.89720786_89720788delinsTCT	GRCh37
NC_000010.9:g.89710766_89710768delinsTCT	NCBI36
NG_007466.2:g.102591_102593delinsTCT , LRG_311:g.102591_102593delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1030_1032delinsTCT	ENSP00000514759.2:p.Lys344Ser
ENST00000710265.1:c.937_939delinsTCT	ENSP00000518161.1:p.Lys313Ser
ENST00000472832.3:c.937_939delinsTCT	ENSP00000483066.2:p.Lys313Ser
ENST00000688158.2:n.1672_1674delinsTCT
ENST00000688922.2:c.*767_*769delinsTCT	ENSP00000508742.2:n.*767_*769delinsTCT
ENST00000700021.1:c.892_894delinsTCT	ENSP00000514757.1:p.Lys298Ser
ENST00000700022.1:c.*276_*278delinsTCT	ENSP00000514758.1:n.*276_*278delinsTCT
ENST00000700023.1:n.2095_2097delinsTCT
ENST00000700024.1:n.2329_2331delinsTCT
ENST00000700025.1:n.1706_1708delinsTCT
ENST00000700026.1:n.574_576delinsTCT
ENST00000706954.1:c.937_939delinsTCT	ENSP00000516674.1:p.Lys313Ser
ENST00000706955.1:c.*972_*974delinsTCT	ENSP00000516675.1:n.*972_*974delinsTCT
ENST00000686459.1:c.*523_*525delinsTCT	ENSP00000508909.1:n.*523_*525delinsTCT
ENST00000688158.1:c.*1048_*1050delinsTCT	ENSP00000509254.1:n.*1048_*1050delinsTCT
ENST00000688308.1:c.937_939delinsTCT	ENSP00000508752.1:p.Lys313Ser
ENST00000688922.1:c.858_860delinsTCT
ENST00000693560.1:c.1456_1458delinsTCT	ENSP00000509861.1:p.Lys486Ser
ENST00000371953.8:c.937_939delinsTCT MANE Select	ENSP00000361021.3:p.Lys313Ser
ENST00000371953.7:c.937_939delinsTCT	ENSP00000361021.3:p.Lys313Ser
ENST00000472832.2:c.364_366delinsTCT	ENSP00000483066.1:p.Lys122Ser
NM_000314.5:c.937_939delinsTCT	NP_000305.3:p.Lys313Ser
NM_000314.6:c.937_939delinsTCT	NP_000305.3:p.Lys313Ser
NM_001304717.2:c.1456_1458delinsTCT	NP_001291646.2:p.Lys486Ser
NM_001304718.1:c.346_348delinsTCT	NP_001291647.1:p.Lys116Ser
XM_006717926.2:c.892_894delinsTCT	XP_006717989.1:p.Lys298Ser
XM_011539981.1:c.937_939delinsTCT	XP_011538283.1:p.Lys313Ser
XM_011539982.1:c.841_843delinsTCT	XP_011538284.1:p.Lys281Ser
XR_945791.1:n.1507_1509delinsTCT
NM_000314.7:c.937_939delinsTCT	NP_000305.3:p.Lys313Ser
NM_001304717.5:c.1456_1458delinsTCT	NP_001291646.4:p.Lys486Ser
NM_001304718.2:c.346_348delinsTCT	NP_001291647.1:p.Lys116Ser
NM_000314.8:c.937_939delinsTCT MANE Select	NP_000305.3:p.Lys313Ser