Canonical Allele Identifier: CA891841060

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960930_87960932delinsATA , CM000672.2:g.87960930_87960932delinsATA	GRCh38
NC_000010.10:g.89720687_89720689delinsATA , CM000672.1:g.89720687_89720689delinsATA	GRCh37
NC_000010.9:g.89710667_89710669delinsATA	NCBI36
NG_007466.2:g.102492_102494delinsATA , LRG_311:g.102492_102494delinsATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.931_933delinsATA	ENSP00000514759.2:p.Ile311=
ENST00000710265.1:c.838_840delinsATA	ENSP00000518161.1:p.Ile280=
ENST00000472832.3:c.838_840delinsATA	ENSP00000483066.2:p.Ile280=
ENST00000688158.2:n.1573_1575delinsATA
ENST00000688922.2:c.*668_*670delinsATA	ENSP00000508742.2:n.*668_*670delinsATA
ENST00000700021.1:c.793_795delinsATA	ENSP00000514757.1:p.Ile265=
ENST00000700022.1:c.*177_*179delinsATA	ENSP00000514758.1:n.*177_*179delinsATA
ENST00000700023.1:n.1996_1998delinsATA
ENST00000700024.1:n.2230_2232delinsATA
ENST00000700025.1:n.1607_1609delinsATA
ENST00000700026.1:n.475_477delinsATA
ENST00000700029.1:c.765_767delinsATA
ENST00000706954.1:c.838_840delinsATA	ENSP00000516674.1:p.Ile280=
ENST00000706955.1:c.*873_*875delinsATA	ENSP00000516675.1:n.*873_*875delinsATA
ENST00000686459.1:c.*424_*426delinsATA	ENSP00000508909.1:n.*424_*426delinsATA
ENST00000688158.1:c.*949_*951delinsATA	ENSP00000509254.1:n.*949_*951delinsATA
ENST00000688308.1:c.838_840delinsATA	ENSP00000508752.1:p.Ile280=
ENST00000688922.1:c.759_761delinsATA
ENST00000693560.1:c.1357_1359delinsATA	ENSP00000509861.1:p.Ile453=
ENST00000371953.8:c.838_840delinsATA MANE Select	ENSP00000361021.3:p.Ile280=
ENST00000371953.7:c.838_840delinsATA	ENSP00000361021.3:p.Ile280=
ENST00000472832.2:c.265_267delinsATA	ENSP00000483066.1:p.Ile89=
NM_000314.5:c.838_840delinsATA	NP_000305.3:p.Ile280=
NM_000314.6:c.838_840delinsATA	NP_000305.3:p.Ile280=
NM_001304717.2:c.1357_1359delinsATA	NP_001291646.2:p.Ile453=
NM_001304718.1:c.247_249delinsATA	NP_001291647.1:p.Ile83=
XM_006717926.2:c.793_795delinsATA	XP_006717989.1:p.Ile265=
XM_011539981.1:c.838_840delinsATA	XP_011538283.1:p.Ile280=
XM_011539982.1:c.742_744delinsATA	XP_011538284.1:p.Ile248=
XR_945791.1:n.1408_1410delinsATA
NM_000314.7:c.838_840delinsATA	NP_000305.3:p.Ile280=
NM_001304717.5:c.1357_1359delinsATA	NP_001291646.4:p.Ile453=
NM_001304718.2:c.247_249delinsATA	NP_001291647.1:p.Ile83=
NM_000314.8:c.838_840delinsATA MANE Select	NP_000305.3:p.Ile280=