Canonical Allele Identifier: CA2695203393

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952137_87952138insACA , CM000672.2:g.87952137_87952138insACA	GRCh38
NC_000010.10:g.89711894_89711895insACA , CM000672.1:g.89711894_89711895insACA	GRCh37
NC_000010.9:g.89701874_89701875insACA	NCBI36
NG_007466.2:g.93699_93700insACA , LRG_311:g.93699_93700insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.512_513insACA	ENSP00000514759.2:p.Gln171_Arg172insGln
ENST00000710265.1:c.512_513insACA	ENSP00000518161.1:p.Gln171_Arg172insGln
ENST00000472832.3:c.512_513insACA	ENSP00000483066.2:p.Gln171_Arg172insGln
ENST00000688158.2:n.1247_1248insACA
ENST00000688922.2:c.*342_*343insACA	ENSP00000508742.2:n.*342_*343insACA
ENST00000700021.1:c.467_468insACA	ENSP00000514757.1:p.Gln156_Arg157insGln
ENST00000700022.1:c.493-5716_493-5715insACA	ENSP00000514758.1:n.493-5716_493-5715insACA
ENST00000700023.1:n.1670_1671insACA
ENST00000700024.1:n.1904_1905insACA
ENST00000700025.1:n.1281_1282insACA
ENST00000700029.1:c.346_347insACA
ENST00000706954.1:c.512_513insACA	ENSP00000516674.1:p.Gln171_Arg172insGln
ENST00000706955.1:c.*547_*548insACA	ENSP00000516675.1:n.*547_*548insACA
ENST00000686459.1:c.*98_*99insACA	ENSP00000508909.1:n.*98_*99insACA
ENST00000688158.1:c.*623_*624insACA	ENSP00000509254.1:n.*623_*624insACA
ENST00000688308.1:c.512_513insACA	ENSP00000508752.1:p.Gln171_Arg172insGln
ENST00000688922.1:c.433_434insACA
ENST00000693560.1:c.1031_1032insACA	ENSP00000509861.1:p.Gln344_Arg345insGln
ENST00000371953.8:c.512_513insACA MANE Select	ENSP00000361021.3:p.Gln171_Arg172insGln
ENST00000371953.7:c.512_513insACA	ENSP00000361021.3:p.Gln171_Arg172insGln
NM_000314.5:c.512_513insACA	NP_000305.3:p.Gln171_Arg172insGln
NM_000314.6:c.512_513insACA	NP_000305.3:p.Gln171_Arg172insGln
NM_001304717.2:c.1031_1032insACA	NP_001291646.2:p.Gln344_Arg345insGln
NM_001304718.1:c.-80_-79insACA	NP_001291647.1:n.-80_-79insACA
XM_006717926.2:c.467_468insACA	XP_006717989.1:p.Gln156_Arg157insGln
XM_011539981.1:c.512_513insACA	XP_011538283.1:p.Gln171_Arg172insGln
XM_011539982.1:c.416_417insACA	XP_011538284.1:p.Gln139_Arg140insGln
XR_945789.1:n.1383_1384insACA
XR_945790.1:n.1500_1501insACA
XR_945791.1:n.1205-5716_1205-5715insACA
NM_000314.7:c.512_513insACA	NP_000305.3:p.Gln171_Arg172insGln
NM_001304717.5:c.1031_1032insACA	NP_001291646.4:p.Gln344_Arg345insGln
NM_001304718.2:c.-80_-79insACA	NP_001291647.1:n.-80_-79insACA
NM_000314.8:c.512_513insACA MANE Select	NP_000305.3:p.Gln171_Arg172insGln