Canonical Allele Identifier: CA1926175665

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966890_87966894delinsTGAAA , CM000672.2:g.87966890_87966894delinsTGAAA	GRCh38
NC_000010.10:g.89726647_89726651delinsTGAAA , CM000672.1:g.89726647_89726651delinsTGAAA	GRCh37
NC_000010.9:g.89716627_89716631delinsTGAAA	NCBI36
NG_007466.2:g.108452_108456delinsTGAAA , LRG_311:g.108452_108456delinsTGAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1659_*1663delinsTGAAA	ENSP00000518161.1:n.*1659_*1663delinsTGAA...
ENST00000688158.2:n.3365_3369delinsTGAAA
ENST00000706954.1:c.*1418_*1422delinsTGAAA	ENSP00000516674.1:n.*1418_*1422delinsTGAA...
ENST00000706955.1:c.*2665_*2669delinsTGAAA	ENSP00000516675.1:n.*2665_*2669delinsTGAA...
ENST00000688158.1:c.*2741_*2745delinsTGAAA	ENSP00000509254.1:n.*2741_*2745delinsTGAA...
ENST00000693560.1:c.*1418_*1422delinsTGAAA	ENSP00000509861.1:n.*1418_*1422delinsTGAA...
ENST00000371953.8:c.*1418_*1422delinsTGAAA MANE Select	ENSP00000361021.3:n.*1418_*1422delinsTGAA...
ENST00000371953.7:c.*1418_*1422delinsTGAAA	ENSP00000361021.3:n.*1418_*1422delinsTGAA...
NM_000314.5:c.*1418_*1422delinsTGAAA	NP_000305.3:n.*1418_*1422delinsTGAAA
NM_000314.6:c.*1418_*1422delinsTGAAA	NP_000305.3:n.*1418_*1422delinsTGAAA
NM_001304717.2:c.*1418_*1422delinsTGAAA	NP_001291646.2:n.*1418_*1422delinsTGAAA
NM_001304718.1:c.*1418_*1422delinsTGAAA	NP_001291647.1:n.*1418_*1422delinsTGAAA
XM_006717926.2:c.*1418_*1422delinsTGAAA	XP_006717989.1:n.*1418_*1422delinsTGAAA
XM_011539982.1:c.*1418_*1422delinsTGAAA	XP_011538284.1:n.*1418_*1422delinsTGAAA
XR_945791.1:n.3200_3204delinsTGAAA
NM_000314.7:c.*1418_*1422delinsTGAAA	NP_000305.3:n.*1418_*1422delinsTGAAA
NM_001304717.5:c.*1418_*1422delinsTGAAA	NP_001291646.4:n.*1418_*1422delinsTGAAA
NM_001304718.2:c.*1418_*1422delinsTGAAA	NP_001291647.1:n.*1418_*1422delinsTGAAA
NM_000314.8:c.*1418_*1422delinsTGAAA MANE Select	NP_000305.3:n.*1418_*1422delinsTGAAA