Canonical Allele Identifier: CA891841664

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965428_87965429delinsTT , CM000672.2:g.87965428_87965429delinsTT	GRCh38
NC_000010.10:g.89725185_89725186delinsTT , CM000672.1:g.89725185_89725186delinsTT	GRCh37
NC_000010.9:g.89715165_89715166delinsTT	NCBI36
NG_007466.2:g.106990_106991delinsTT , LRG_311:g.106990_106991delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1261_1262delinsTT	ENSP00000514759.2:p.Glu421Leu
ENST00000710265.1:c.*197_*198delinsTT	ENSP00000518161.1:n.*197_*198delinsTT
ENST00000688158.2:n.1903_1904delinsTT
ENST00000688922.2:c.*998_*999delinsTT	ENSP00000508742.2:n.*998_*999delinsTT
ENST00000700021.1:c.1123_1124delinsTT	ENSP00000514757.1:p.Glu375Leu
ENST00000700022.1:c.*507_*508delinsTT	ENSP00000514758.1:n.*507_*508delinsTT
ENST00000700023.1:n.2326_2327delinsTT
ENST00000700024.1:n.2560_2561delinsTT
ENST00000706954.1:c.1168_1169delinsTT	ENSP00000516674.1:p.Glu390Leu
ENST00000706955.1:c.*1203_*1204delinsTT	ENSP00000516675.1:n.*1203_*1204delinsTT
ENST00000686459.1:c.*754_*755delinsTT	ENSP00000508909.1:n.*754_*755delinsTT
ENST00000688158.1:c.*1279_*1280delinsTT	ENSP00000509254.1:n.*1279_*1280delinsTT
ENST00000688308.1:c.1168_1169delinsTT	ENSP00000508752.1:p.Glu390Leu
ENST00000688922.1:c.1089_1090delinsTT
ENST00000693560.1:c.1687_1688delinsTT	ENSP00000509861.1:p.Glu563Leu
ENST00000371953.8:c.1168_1169delinsTT MANE Select	ENSP00000361021.3:p.Glu390Leu
ENST00000371953.7:c.1168_1169delinsTT	ENSP00000361021.3:p.Glu390Leu
NM_000314.5:c.1168_1169delinsTT	NP_000305.3:p.Glu390Leu
NM_000314.6:c.1168_1169delinsTT	NP_000305.3:p.Glu390Leu
NM_001304717.2:c.1687_1688delinsTT	NP_001291646.2:p.Glu563Leu
NM_001304718.1:c.577_578delinsTT	NP_001291647.1:p.Glu193Leu
XM_006717926.2:c.1123_1124delinsTT	XP_006717989.1:p.Glu375Leu
XM_011539982.1:c.1072_1073delinsTT	XP_011538284.1:p.Glu358Leu
XR_945791.1:n.1738_1739delinsTT
NM_000314.7:c.1168_1169delinsTT	NP_000305.3:p.Glu390Leu
NM_001304717.5:c.1687_1688delinsTT	NP_001291646.4:p.Glu563Leu
NM_001304718.2:c.577_578delinsTT	NP_001291647.1:p.Glu193Leu
NM_000314.8:c.1168_1169delinsTT MANE Select	NP_000305.3:p.Glu390Leu