Canonical Allele Identifier: CA891841459

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965287_87965288delinsTA , CM000672.2:g.87965287_87965288delinsTA	GRCh38
NC_000010.10:g.89725044_89725045delinsTA , CM000672.1:g.89725044_89725045delinsTA	GRCh37
NC_000010.9:g.89715024_89715025delinsTA	NCBI36
NG_007466.2:g.106849_106850delinsTA , LRG_311:g.106849_106850delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120_1121delinsTA	ENSP00000514759.2:p.Val374Ter
ENST00000710265.1:c.*56_*57delinsTA	ENSP00000518161.1:n.*56_*57delinsTA
ENST00000688158.2:n.1762_1763delinsTA
ENST00000688922.2:c.*857_*858delinsTA	ENSP00000508742.2:n.*857_*858delinsTA
ENST00000700021.1:c.982_983delinsTA	ENSP00000514757.1:p.Val328Ter
ENST00000700022.1:c.*366_*367delinsTA	ENSP00000514758.1:n.*366_*367delinsTA
ENST00000700023.1:n.2185_2186delinsTA
ENST00000700024.1:n.2419_2420delinsTA
ENST00000706954.1:c.1027_1028delinsTA	ENSP00000516674.1:p.Val343Ter
ENST00000706955.1:c.*1062_*1063delinsTA	ENSP00000516675.1:n.*1062_*1063delinsTA
ENST00000686459.1:c.*613_*614delinsTA	ENSP00000508909.1:n.*613_*614delinsTA
ENST00000688158.1:c.*1138_*1139delinsTA	ENSP00000509254.1:n.*1138_*1139delinsTA
ENST00000688308.1:c.1027_1028delinsTA	ENSP00000508752.1:p.Val343Ter
ENST00000688922.1:c.948_949delinsTA
ENST00000693560.1:c.1546_1547delinsTA	ENSP00000509861.1:p.Val516Ter
ENST00000371953.8:c.1027_1028delinsTA MANE Select	ENSP00000361021.3:p.Val343Ter
ENST00000371953.7:c.1027_1028delinsTA	ENSP00000361021.3:p.Val343Ter
NM_000314.5:c.1027_1028delinsTA	NP_000305.3:p.Val343Ter
NM_000314.6:c.1027_1028delinsTA	NP_000305.3:p.Val343Ter
NM_001304717.2:c.1546_1547delinsTA	NP_001291646.2:p.Val516Ter
NM_001304718.1:c.436_437delinsTA	NP_001291647.1:p.Val146Ter
XM_006717926.2:c.982_983delinsTA	XP_006717989.1:p.Val328Ter
XM_011539982.1:c.931_932delinsTA	XP_011538284.1:p.Val311Ter
XR_945791.1:n.1597_1598delinsTA
NM_000314.7:c.1027_1028delinsTA	NP_000305.3:p.Val343Ter
NM_001304717.5:c.1546_1547delinsTA	NP_001291646.4:p.Val516Ter
NM_001304718.2:c.436_437delinsTA	NP_001291647.1:p.Val146Ter
NM_000314.8:c.1027_1028delinsTA MANE Select	NP_000305.3:p.Val343Ter