Canonical Allele Identifier: CA891836985

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965287_87965288delinsTG , CM000672.2:g.87965287_87965288delinsTG	GRCh38
NC_000010.10:g.89725044_89725045delinsTG , CM000672.1:g.89725044_89725045delinsTG	GRCh37
NC_000010.9:g.89715024_89715025delinsTG	NCBI36
NG_007466.2:g.106849_106850delinsTG , LRG_311:g.106849_106850delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120_1121delinsTG	ENSP00000514759.2:p.Val374Trp
ENST00000710265.1:c.*56_*57delinsTG	ENSP00000518161.1:n.*56_*57delinsTG
ENST00000688158.2:n.1762_1763delinsTG
ENST00000688922.2:c.*857_*858delinsTG	ENSP00000508742.2:n.*857_*858delinsTG
ENST00000700021.1:c.982_983delinsTG	ENSP00000514757.1:p.Val328Trp
ENST00000700022.1:c.*366_*367delinsTG	ENSP00000514758.1:n.*366_*367delinsTG
ENST00000700023.1:n.2185_2186delinsTG
ENST00000700024.1:n.2419_2420delinsTG
ENST00000706954.1:c.1027_1028delinsTG	ENSP00000516674.1:p.Val343Trp
ENST00000706955.1:c.*1062_*1063delinsTG	ENSP00000516675.1:n.*1062_*1063delinsTG
ENST00000686459.1:c.*613_*614delinsTG	ENSP00000508909.1:n.*613_*614delinsTG
ENST00000688158.1:c.*1138_*1139delinsTG	ENSP00000509254.1:n.*1138_*1139delinsTG
ENST00000688308.1:c.1027_1028delinsTG	ENSP00000508752.1:p.Val343Trp
ENST00000688922.1:c.948_949delinsTG
ENST00000693560.1:c.1546_1547delinsTG	ENSP00000509861.1:p.Val516Trp
ENST00000371953.8:c.1027_1028delinsTG MANE Select	ENSP00000361021.3:p.Val343Trp
ENST00000371953.7:c.1027_1028delinsTG	ENSP00000361021.3:p.Val343Trp
NM_000314.5:c.1027_1028delinsTG	NP_000305.3:p.Val343Trp
NM_000314.6:c.1027_1028delinsTG	NP_000305.3:p.Val343Trp
NM_001304717.2:c.1546_1547delinsTG	NP_001291646.2:p.Val516Trp
NM_001304718.1:c.436_437delinsTG	NP_001291647.1:p.Val146Trp
XM_006717926.2:c.982_983delinsTG	XP_006717989.1:p.Val328Trp
XM_011539982.1:c.931_932delinsTG	XP_011538284.1:p.Val311Trp
XR_945791.1:n.1597_1598delinsTG
NM_000314.7:c.1027_1028delinsTG	NP_000305.3:p.Val343Trp
NM_001304717.5:c.1546_1547delinsTG	NP_001291646.4:p.Val516Trp
NM_001304718.2:c.436_437delinsTG	NP_001291647.1:p.Val146Trp
NM_000314.8:c.1027_1028delinsTG MANE Select	NP_000305.3:p.Val343Trp