Canonical Allele Identifier: CA2579926604

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961101_87961103delinsCCA , CM000672.2:g.87961101_87961103delinsCCA	GRCh38
NC_000010.10:g.89720858_89720860delinsCCA , CM000672.1:g.89720858_89720860delinsCCA	GRCh37
NC_000010.9:g.89710838_89710840delinsCCA	NCBI36
NG_007466.2:g.102663_102665delinsCCA , LRG_311:g.102663_102665delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1102_1104delinsCCA	ENSP00000514759.2:p.Phe368Pro
ENST00000710265.1:c.1009_1011delinsCCA	ENSP00000518161.1:p.Phe337Pro
ENST00000472832.3:c.1009_1011delinsCCA	ENSP00000483066.2:p.Phe337Pro
ENST00000688158.2:n.1744_1746delinsCCA
ENST00000688922.2:c.*839_*841delinsCCA	ENSP00000508742.2:n.*839_*841delinsCCA
ENST00000700021.1:c.964_966delinsCCA	ENSP00000514757.1:p.Phe322Pro
ENST00000700022.1:c.*348_*350delinsCCA	ENSP00000514758.1:n.*348_*350delinsCCA
ENST00000700023.1:n.2167_2169delinsCCA
ENST00000700024.1:n.2401_2403delinsCCA
ENST00000700025.1:n.1778_1780delinsCCA
ENST00000700026.1:n.646_648delinsCCA
ENST00000706954.1:c.1009_1011delinsCCA	ENSP00000516674.1:p.Phe337Pro
ENST00000706955.1:c.*1044_*1046delinsCCA	ENSP00000516675.1:n.*1044_*1046delinsCCA
ENST00000686459.1:c.*595_*597delinsCCA	ENSP00000508909.1:n.*595_*597delinsCCA
ENST00000688158.1:c.*1120_*1122delinsCCA	ENSP00000509254.1:n.*1120_*1122delinsCCA
ENST00000688308.1:c.1009_1011delinsCCA	ENSP00000508752.1:p.Phe337Pro
ENST00000688922.1:c.930_932delinsCCA
ENST00000693560.1:c.1528_1530delinsCCA	ENSP00000509861.1:p.Phe510Pro
ENST00000371953.8:c.1009_1011delinsCCA MANE Select	ENSP00000361021.3:p.Phe337Pro
ENST00000371953.7:c.1009_1011delinsCCA	ENSP00000361021.3:p.Phe337Pro
ENST00000472832.2:c.436_438delinsCCA	ENSP00000483066.1:p.Phe146Pro
NM_000314.5:c.1009_1011delinsCCA	NP_000305.3:p.Phe337Pro
NM_000314.6:c.1009_1011delinsCCA	NP_000305.3:p.Phe337Pro
NM_001304717.2:c.1528_1530delinsCCA	NP_001291646.2:p.Phe510Pro
NM_001304718.1:c.418_420delinsCCA	NP_001291647.1:p.Phe140Pro
XM_006717926.2:c.964_966delinsCCA	XP_006717989.1:p.Phe322Pro
XM_011539981.1:c.1009_1011delinsCCA	XP_011538283.1:p.Phe337Pro
XM_011539982.1:c.913_915delinsCCA	XP_011538284.1:p.Phe305Pro
XR_945791.1:n.1579_1581delinsCCA
NM_000314.7:c.1009_1011delinsCCA	NP_000305.3:p.Phe337Pro
NM_001304717.5:c.1528_1530delinsCCA	NP_001291646.4:p.Phe510Pro
NM_001304718.2:c.418_420delinsCCA	NP_001291647.1:p.Phe140Pro
NM_000314.8:c.1009_1011delinsCCA MANE Select	NP_000305.3:p.Phe337Pro