Canonical Allele Identifier: CA891836574

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933045_87933047delinsATG , CM000672.2:g.87933045_87933047delinsATG	GRCh38
NC_000010.10:g.89692802_89692804delinsATG , CM000672.1:g.89692802_89692804delinsATG	GRCh37
NC_000010.9:g.89682782_89682784delinsATG	NCBI36
NG_007466.2:g.74607_74609delinsATG , LRG_311:g.74607_74609delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.286_288delinsATG	ENSP00000514759.2:p.Pro96Met
ENST00000710265.1:c.286_288delinsATG	ENSP00000518161.1:p.Pro96Met
ENST00000472832.3:c.286_288delinsATG	ENSP00000483066.2:p.Pro96Met
ENST00000688158.2:n.1021_1023delinsATG
ENST00000688922.2:c.*116_*118delinsATG	ENSP00000508742.2:n.*116_*118delinsATG
ENST00000700021.1:c.241_243delinsATG	ENSP00000514757.1:p.Pro81Met
ENST00000700022.1:c.286_288delinsATG	ENSP00000514758.1:p.Pro96Met
ENST00000700029.1:c.120_122delinsATG
ENST00000706954.1:c.286_288delinsATG	ENSP00000516674.1:p.Pro96Met
ENST00000706955.1:c.*321_*323delinsATG	ENSP00000516675.1:n.*321_*323delinsATG
ENST00000686459.1:c.286_288delinsATG	ENSP00000508909.1:p.Pro96Met
ENST00000688158.1:c.*397_*399delinsATG	ENSP00000509254.1:n.*397_*399delinsATG
ENST00000688308.1:c.286_288delinsATG	ENSP00000508752.1:p.Pro96Met
ENST00000688922.1:c.207_209delinsATG
ENST00000693560.1:c.805_807delinsATG	ENSP00000509861.1:p.Pro269Met
ENST00000371953.8:c.286_288delinsATG MANE Select	ENSP00000361021.3:p.Pro96Met
ENST00000371953.7:c.286_288delinsATG	ENSP00000361021.3:p.Pro96Met
ENST00000498703.1:n.112_114delinsATG
ENST00000610634.1:c.184_186delinsATG	ENSP00000477517.1:p.Pro62Met
NM_000314.5:c.286_288delinsATG	NP_000305.3:p.Pro96Met
NM_000314.6:c.286_288delinsATG	NP_000305.3:p.Pro96Met
NM_001304717.2:c.805_807delinsATG	NP_001291646.2:p.Pro269Met
NM_001304718.1:c.-465_-463delinsATG	NP_001291647.1:n.-465_-463delinsATG
XM_006717926.2:c.241_243delinsATG	XP_006717989.1:p.Pro81Met
XM_011539981.1:c.286_288delinsATG	XP_011538283.1:p.Pro96Met
XM_011539982.1:c.190_192delinsATG	XP_011538284.1:p.Pro64Met
XR_945789.1:n.998_1000delinsATG
XR_945790.1:n.998_1000delinsATG
XR_945791.1:n.998_1000delinsATG
NM_000314.7:c.286_288delinsATG	NP_000305.3:p.Pro96Met
NM_001304717.5:c.805_807delinsATG	NP_001291646.4:p.Pro269Met
NM_001304718.2:c.-465_-463delinsATG	NP_001291647.1:n.-465_-463delinsATG
NM_000314.8:c.286_288delinsATG MANE Select	NP_000305.3:p.Pro96Met