Canonical Allele Identifier: CA891841026

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960915_87960916delinsCG , CM000672.2:g.87960915_87960916delinsCG	GRCh38
NC_000010.10:g.89720672_89720673delinsCG , CM000672.1:g.89720672_89720673delinsCG	GRCh37
NC_000010.9:g.89710652_89710653delinsCG	NCBI36
NG_007466.2:g.102477_102478delinsCG , LRG_311:g.102477_102478delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.916_917delinsCG	ENSP00000514759.2:p.Val306Arg
ENST00000710265.1:c.823_824delinsCG	ENSP00000518161.1:p.Val275Arg
ENST00000472832.3:c.823_824delinsCG	ENSP00000483066.2:p.Val275Arg
ENST00000688158.2:n.1558_1559delinsCG
ENST00000688922.2:c.*653_*654delinsCG	ENSP00000508742.2:n.*653_*654delinsCG
ENST00000700021.1:c.778_779delinsCG	ENSP00000514757.1:p.Val260Arg
ENST00000700022.1:c.*162_*163delinsCG	ENSP00000514758.1:n.*162_*163delinsCG
ENST00000700023.1:n.1981_1982delinsCG
ENST00000700024.1:n.2215_2216delinsCG
ENST00000700025.1:n.1592_1593delinsCG
ENST00000700026.1:n.460_461delinsCG
ENST00000700029.1:c.750_751delinsCG
ENST00000706954.1:c.823_824delinsCG	ENSP00000516674.1:p.Val275Arg
ENST00000706955.1:c.*858_*859delinsCG	ENSP00000516675.1:n.*858_*859delinsCG
ENST00000686459.1:c.*409_*410delinsCG	ENSP00000508909.1:n.*409_*410delinsCG
ENST00000688158.1:c.*934_*935delinsCG	ENSP00000509254.1:n.*934_*935delinsCG
ENST00000688308.1:c.823_824delinsCG	ENSP00000508752.1:p.Val275Arg
ENST00000688922.1:c.744_745delinsCG
ENST00000693560.1:c.1342_1343delinsCG	ENSP00000509861.1:p.Val448Arg
ENST00000371953.8:c.823_824delinsCG MANE Select	ENSP00000361021.3:p.Val275Arg
ENST00000371953.7:c.823_824delinsCG	ENSP00000361021.3:p.Val275Arg
ENST00000472832.2:c.250_251delinsCG	ENSP00000483066.1:p.Val84Arg
NM_000314.5:c.823_824delinsCG	NP_000305.3:p.Val275Arg
NM_000314.6:c.823_824delinsCG	NP_000305.3:p.Val275Arg
NM_001304717.2:c.1342_1343delinsCG	NP_001291646.2:p.Val448Arg
NM_001304718.1:c.232_233delinsCG	NP_001291647.1:p.Val78Arg
XM_006717926.2:c.778_779delinsCG	XP_006717989.1:p.Val260Arg
XM_011539981.1:c.823_824delinsCG	XP_011538283.1:p.Val275Arg
XM_011539982.1:c.727_728delinsCG	XP_011538284.1:p.Val243Arg
XR_945791.1:n.1393_1394delinsCG
NM_000314.7:c.823_824delinsCG	NP_000305.3:p.Val275Arg
NM_001304717.5:c.1342_1343delinsCG	NP_001291646.4:p.Val448Arg
NM_001304718.2:c.232_233delinsCG	NP_001291647.1:p.Val78Arg
NM_000314.8:c.823_824delinsCG MANE Select	NP_000305.3:p.Val275Arg