Canonical Allele Identifier: CA891840243

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960912_87960913delinsAT , CM000672.2:g.87960912_87960913delinsAT	GRCh38
NC_000010.10:g.89720669_89720670delinsAT , CM000672.1:g.89720669_89720670delinsAT	GRCh37
NC_000010.9:g.89710649_89710650delinsAT	NCBI36
NG_007466.2:g.102474_102475delinsAT , LRG_311:g.102474_102475delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.913_914delinsAT	ENSP00000514759.2:p.Trp305Met
ENST00000710265.1:c.820_821delinsAT	ENSP00000518161.1:p.Trp274Met
ENST00000472832.3:c.820_821delinsAT	ENSP00000483066.2:p.Trp274Met
ENST00000688158.2:n.1555_1556delinsAT
ENST00000688922.2:c.*650_*651delinsAT	ENSP00000508742.2:n.*650_*651delinsAT
ENST00000700021.1:c.775_776delinsAT	ENSP00000514757.1:p.Trp259Met
ENST00000700022.1:c.*159_*160delinsAT	ENSP00000514758.1:n.*159_*160delinsAT
ENST00000700023.1:n.1978_1979delinsAT
ENST00000700024.1:n.2212_2213delinsAT
ENST00000700025.1:n.1589_1590delinsAT
ENST00000700026.1:n.457_458delinsAT
ENST00000700029.1:c.747_748delinsAT
ENST00000706954.1:c.820_821delinsAT	ENSP00000516674.1:p.Trp274Met
ENST00000706955.1:c.*855_*856delinsAT	ENSP00000516675.1:n.*855_*856delinsAT
ENST00000686459.1:c.*406_*407delinsAT	ENSP00000508909.1:n.*406_*407delinsAT
ENST00000688158.1:c.*931_*932delinsAT	ENSP00000509254.1:n.*931_*932delinsAT
ENST00000688308.1:c.820_821delinsAT	ENSP00000508752.1:p.Trp274Met
ENST00000688922.1:c.741_742delinsAT
ENST00000693560.1:c.1339_1340delinsAT	ENSP00000509861.1:p.Trp447Met
ENST00000371953.8:c.820_821delinsAT MANE Select	ENSP00000361021.3:p.Trp274Met
ENST00000371953.7:c.820_821delinsAT	ENSP00000361021.3:p.Trp274Met
ENST00000472832.2:c.247_248delinsAT	ENSP00000483066.1:p.Trp83Met
NM_000314.5:c.820_821delinsAT	NP_000305.3:p.Trp274Met
NM_000314.6:c.820_821delinsAT	NP_000305.3:p.Trp274Met
NM_001304717.2:c.1339_1340delinsAT	NP_001291646.2:p.Trp447Met
NM_001304718.1:c.229_230delinsAT	NP_001291647.1:p.Trp77Met
XM_006717926.2:c.775_776delinsAT	XP_006717989.1:p.Trp259Met
XM_011539981.1:c.820_821delinsAT	XP_011538283.1:p.Trp274Met
XM_011539982.1:c.724_725delinsAT	XP_011538284.1:p.Trp242Met
XR_945791.1:n.1390_1391delinsAT
NM_000314.7:c.820_821delinsAT	NP_000305.3:p.Trp274Met
NM_001304717.5:c.1339_1340delinsAT	NP_001291646.4:p.Trp447Met
NM_001304718.2:c.229_230delinsAT	NP_001291647.1:p.Trp77Met
NM_000314.8:c.820_821delinsAT MANE Select	NP_000305.3:p.Trp274Met