Canonical Allele Identifier: CA891841013

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960912_87960913delinsAC , CM000672.2:g.87960912_87960913delinsAC	GRCh38
NC_000010.10:g.89720669_89720670delinsAC , CM000672.1:g.89720669_89720670delinsAC	GRCh37
NC_000010.9:g.89710649_89710650delinsAC	NCBI36
NG_007466.2:g.102474_102475delinsAC , LRG_311:g.102474_102475delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.913_914delinsAC	ENSP00000514759.2:p.Trp305Thr
ENST00000710265.1:c.820_821delinsAC	ENSP00000518161.1:p.Trp274Thr
ENST00000472832.3:c.820_821delinsAC	ENSP00000483066.2:p.Trp274Thr
ENST00000688158.2:n.1555_1556delinsAC
ENST00000688922.2:c.*650_*651delinsAC	ENSP00000508742.2:n.*650_*651delinsAC
ENST00000700021.1:c.775_776delinsAC	ENSP00000514757.1:p.Trp259Thr
ENST00000700022.1:c.*159_*160delinsAC	ENSP00000514758.1:n.*159_*160delinsAC
ENST00000700023.1:n.1978_1979delinsAC
ENST00000700024.1:n.2212_2213delinsAC
ENST00000700025.1:n.1589_1590delinsAC
ENST00000700026.1:n.457_458delinsAC
ENST00000700029.1:c.747_748delinsAC
ENST00000706954.1:c.820_821delinsAC	ENSP00000516674.1:p.Trp274Thr
ENST00000706955.1:c.*855_*856delinsAC	ENSP00000516675.1:n.*855_*856delinsAC
ENST00000686459.1:c.*406_*407delinsAC	ENSP00000508909.1:n.*406_*407delinsAC
ENST00000688158.1:c.*931_*932delinsAC	ENSP00000509254.1:n.*931_*932delinsAC
ENST00000688308.1:c.820_821delinsAC	ENSP00000508752.1:p.Trp274Thr
ENST00000688922.1:c.741_742delinsAC
ENST00000693560.1:c.1339_1340delinsAC	ENSP00000509861.1:p.Trp447Thr
ENST00000371953.8:c.820_821delinsAC MANE Select	ENSP00000361021.3:p.Trp274Thr
ENST00000371953.7:c.820_821delinsAC	ENSP00000361021.3:p.Trp274Thr
ENST00000472832.2:c.247_248delinsAC	ENSP00000483066.1:p.Trp83Thr
NM_000314.5:c.820_821delinsAC	NP_000305.3:p.Trp274Thr
NM_000314.6:c.820_821delinsAC	NP_000305.3:p.Trp274Thr
NM_001304717.2:c.1339_1340delinsAC	NP_001291646.2:p.Trp447Thr
NM_001304718.1:c.229_230delinsAC	NP_001291647.1:p.Trp77Thr
XM_006717926.2:c.775_776delinsAC	XP_006717989.1:p.Trp259Thr
XM_011539981.1:c.820_821delinsAC	XP_011538283.1:p.Trp274Thr
XM_011539982.1:c.724_725delinsAC	XP_011538284.1:p.Trp242Thr
XR_945791.1:n.1390_1391delinsAC
NM_000314.7:c.820_821delinsAC	NP_000305.3:p.Trp274Thr
NM_001304717.5:c.1339_1340delinsAC	NP_001291646.4:p.Trp447Thr
NM_001304718.2:c.229_230delinsAC	NP_001291647.1:p.Trp77Thr
NM_000314.8:c.820_821delinsAC MANE Select	NP_000305.3:p.Trp274Thr