Canonical Allele Identifier: CA891837818

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933159_87933161delinsTCT , CM000672.2:g.87933159_87933161delinsTCT	GRCh38
NC_000010.10:g.89692916_89692918delinsTCT , CM000672.1:g.89692916_89692918delinsTCT	GRCh37
NC_000010.9:g.89682896_89682898delinsTCT	NCBI36
NG_007466.2:g.74721_74723delinsTCT , LRG_311:g.74721_74723delinsTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.400_402delinsTCT	ENSP00000514759.2:p.Met134Ser
ENST00000710265.1:c.400_402delinsTCT	ENSP00000518161.1:p.Met134Ser
ENST00000472832.3:c.400_402delinsTCT	ENSP00000483066.2:p.Met134Ser
ENST00000688158.2:n.1135_1137delinsTCT
ENST00000688922.2:c.*230_*232delinsTCT	ENSP00000508742.2:n.*230_*232delinsTCT
ENST00000700021.1:c.355_357delinsTCT	ENSP00000514757.1:p.Met119Ser
ENST00000700022.1:c.400_402delinsTCT	ENSP00000514758.1:p.Met134Ser
ENST00000700029.1:c.234_236delinsTCT
ENST00000706954.1:c.400_402delinsTCT	ENSP00000516674.1:p.Met134Ser
ENST00000706955.1:c.*435_*437delinsTCT	ENSP00000516675.1:n.*435_*437delinsTCT
ENST00000686459.1:c.400_402delinsTCT	ENSP00000508909.1:p.Met134Ser
ENST00000688158.1:c.*511_*513delinsTCT	ENSP00000509254.1:n.*511_*513delinsTCT
ENST00000688308.1:c.400_402delinsTCT	ENSP00000508752.1:p.Met134Ser
ENST00000688922.1:c.321_323delinsTCT
ENST00000693560.1:c.919_921delinsTCT	ENSP00000509861.1:p.Met307Ser
ENST00000371953.8:c.400_402delinsTCT MANE Select	ENSP00000361021.3:p.Met134Ser
ENST00000371953.7:c.400_402delinsTCT	ENSP00000361021.3:p.Met134Ser
ENST00000498703.1:n.226_228delinsTCT
ENST00000610634.1:c.298_300delinsTCT	ENSP00000477517.1:p.Met100Ser
NM_000314.5:c.400_402delinsTCT	NP_000305.3:p.Met134Ser
NM_000314.6:c.400_402delinsTCT	NP_000305.3:p.Met134Ser
NM_001304717.2:c.919_921delinsTCT	NP_001291646.2:p.Met307Ser
NM_001304718.1:c.-351_-349delinsTCT	NP_001291647.1:n.-351_-349delinsTCT
XM_006717926.2:c.355_357delinsTCT	XP_006717989.1:p.Met119Ser
XM_011539981.1:c.400_402delinsTCT	XP_011538283.1:p.Met134Ser
XM_011539982.1:c.304_306delinsTCT	XP_011538284.1:p.Met102Ser
XR_945789.1:n.1112_1114delinsTCT
XR_945790.1:n.1112_1114delinsTCT
XR_945791.1:n.1112_1114delinsTCT
NM_000314.7:c.400_402delinsTCT	NP_000305.3:p.Met134Ser
NM_001304717.5:c.919_921delinsTCT	NP_001291646.4:p.Met307Ser
NM_001304718.2:c.-351_-349delinsTCT	NP_001291647.1:n.-351_-349delinsTCT
NM_000314.8:c.400_402delinsTCT MANE Select	NP_000305.3:p.Met134Ser