Canonical Allele Identifier: CA645554094

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960978_87960979insA , CM000672.2:g.87960978_87960979insA	GRCh38
NC_000010.10:g.89720735_89720736insA , CM000672.1:g.89720735_89720736insA	GRCh37
NC_000010.9:g.89710715_89710716insA	NCBI36
NG_007466.2:g.102540_102541insA , LRG_311:g.102540_102541insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.979_980insA	ENSP00000514759.2:p.Cys327Ter
ENST00000710265.1:c.886_887insA	ENSP00000518161.1:p.Cys296Ter
ENST00000472832.3:c.886_887insA	ENSP00000483066.2:p.Cys296Ter
ENST00000688158.2:n.1621_1622insA
ENST00000688922.2:c.*716_*717insA	ENSP00000508742.2:n.*716_*717insA
ENST00000700021.1:c.841_842insA	ENSP00000514757.1:p.Cys281Ter
ENST00000700022.1:c.*225_*226insA	ENSP00000514758.1:n.*225_*226insA
ENST00000700023.1:n.2044_2045insA
ENST00000700024.1:n.2278_2279insA
ENST00000700025.1:n.1655_1656insA
ENST00000700026.1:n.523_524insA
ENST00000706954.1:c.886_887insA	ENSP00000516674.1:p.Cys296Ter
ENST00000706955.1:c.*921_*922insA	ENSP00000516675.1:n.*921_*922insA
ENST00000686459.1:c.*472_*473insA	ENSP00000508909.1:n.*472_*473insA
ENST00000688158.1:c.*997_*998insA	ENSP00000509254.1:n.*997_*998insA
ENST00000688308.1:c.886_887insA	ENSP00000508752.1:p.Cys296Ter
ENST00000688922.1:c.807_808insA
ENST00000693560.1:c.1405_1406insA	ENSP00000509861.1:p.Cys469Ter
ENST00000371953.8:c.886_887insA MANE Select	ENSP00000361021.3:p.Cys296Ter
ENST00000371953.7:c.886_887insA	ENSP00000361021.3:p.Cys296Ter
ENST00000472832.2:c.313_314insA	ENSP00000483066.1:p.Cys105Ter
NM_000314.5:c.886_887insA	NP_000305.3:p.Cys296Ter
NM_000314.6:c.886_887insA	NP_000305.3:p.Cys296Ter
NM_001304717.2:c.1405_1406insA	NP_001291646.2:p.Cys469Ter
NM_001304718.1:c.295_296insA	NP_001291647.1:p.Cys99Ter
XM_006717926.2:c.841_842insA	XP_006717989.1:p.Cys281Ter
XM_011539981.1:c.886_887insA	XP_011538283.1:p.Cys296Ter
XM_011539982.1:c.790_791insA	XP_011538284.1:p.Cys264Ter
XR_945791.1:n.1456_1457insA
NM_000314.7:c.886_887insA	NP_000305.3:p.Cys296Ter
NM_001304717.5:c.1405_1406insA	NP_001291646.4:p.Cys469Ter
NM_001304718.2:c.295_296insA	NP_001291647.1:p.Cys99Ter
NM_000314.8:c.886_887insA MANE Select	NP_000305.3:p.Cys296Ter