Canonical Allele Identifier: CA891839968

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957982_87957983delinsAT , CM000672.2:g.87957982_87957983delinsAT	GRCh38
NC_000010.10:g.89717739_89717740delinsAT , CM000672.1:g.89717739_89717740delinsAT	GRCh37
NC_000010.9:g.89707719_89707720delinsAT	NCBI36
NG_007466.2:g.99544_99545delinsAT , LRG_311:g.99544_99545delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.764_765delinsAT	ENSP00000514759.2:p.Val255Asp
ENST00000710265.1:c.764_765delinsAT	ENSP00000518161.1:p.Val255Asp
ENST00000472832.3:c.764_765delinsAT	ENSP00000483066.2:p.Val255Asp
ENST00000688158.2:n.1499_1500delinsAT
ENST00000688922.2:c.*594_*595delinsAT	ENSP00000508742.2:n.*594_*595delinsAT
ENST00000700021.1:c.719_720delinsAT	ENSP00000514757.1:p.Val240Asp
ENST00000700022.1:c.*103_*104delinsAT	ENSP00000514758.1:n.*103_*104delinsAT
ENST00000700023.1:n.1922_1923delinsAT
ENST00000700024.1:n.2156_2157delinsAT
ENST00000700025.1:n.1533_1534delinsAT
ENST00000700026.1:n.401_402delinsAT
ENST00000700029.1:c.598_599delinsAT
ENST00000706954.1:c.764_765delinsAT	ENSP00000516674.1:p.Val255Asp
ENST00000706955.1:c.*799_*800delinsAT	ENSP00000516675.1:n.*799_*800delinsAT
ENST00000686459.1:c.*350_*351delinsAT	ENSP00000508909.1:n.*350_*351delinsAT
ENST00000688158.1:c.*875_*876delinsAT	ENSP00000509254.1:n.*875_*876delinsAT
ENST00000688308.1:c.764_765delinsAT	ENSP00000508752.1:p.Val255Asp
ENST00000688922.1:c.685_686delinsAT
ENST00000693560.1:c.1283_1284delinsAT	ENSP00000509861.1:p.Val428Asp
ENST00000371953.8:c.764_765delinsAT MANE Select	ENSP00000361021.3:p.Val255Asp
ENST00000371953.7:c.764_765delinsAT	ENSP00000361021.3:p.Val255Asp
ENST00000472832.2:c.191_192delinsAT	ENSP00000483066.1:p.Val64Asp
NM_000314.5:c.764_765delinsAT	NP_000305.3:p.Val255Asp
NM_000314.6:c.764_765delinsAT	NP_000305.3:p.Val255Asp
NM_001304717.2:c.1283_1284delinsAT	NP_001291646.2:p.Val428Asp
NM_001304718.1:c.173_174delinsAT	NP_001291647.1:p.Val58Asp
XM_006717926.2:c.719_720delinsAT	XP_006717989.1:p.Val240Asp
XM_011539981.1:c.764_765delinsAT	XP_011538283.1:p.Val255Asp
XM_011539982.1:c.668_669delinsAT	XP_011538284.1:p.Val223Asp
XR_945791.1:n.1334_1335delinsAT
NM_000314.7:c.764_765delinsAT	NP_000305.3:p.Val255Asp
NM_001304717.5:c.1283_1284delinsAT	NP_001291646.4:p.Val428Asp
NM_001304718.2:c.173_174delinsAT	NP_001291647.1:p.Val58Asp
NM_000314.8:c.764_765delinsAT MANE Select	NP_000305.3:p.Val255Asp