Canonical Allele Identifier: CA891841570

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965324_87965325delinsGG , CM000672.2:g.87965324_87965325delinsGG	GRCh38
NC_000010.10:g.89725081_89725082delinsGG , CM000672.1:g.89725081_89725082delinsGG	GRCh37
NC_000010.9:g.89715061_89715062delinsGG	NCBI36
NG_007466.2:g.106886_106887delinsGG , LRG_311:g.106886_106887delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1157_1158delinsGG	ENSP00000514759.2:p.Ser386Trp
ENST00000710265.1:c.*93_*94delinsGG	ENSP00000518161.1:n.*93_*94delinsGG
ENST00000688158.2:n.1799_1800delinsGG
ENST00000688922.2:c.*894_*895delinsGG	ENSP00000508742.2:n.*894_*895delinsGG
ENST00000700021.1:c.1019_1020delinsGG	ENSP00000514757.1:p.Ser340Trp
ENST00000700022.1:c.*403_*404delinsGG	ENSP00000514758.1:n.*403_*404delinsGG
ENST00000700023.1:n.2222_2223delinsGG
ENST00000700024.1:n.2456_2457delinsGG
ENST00000706954.1:c.1064_1065delinsGG	ENSP00000516674.1:p.Ser355Trp
ENST00000706955.1:c.*1099_*1100delinsGG	ENSP00000516675.1:n.*1099_*1100delinsGG
ENST00000686459.1:c.*650_*651delinsGG	ENSP00000508909.1:n.*650_*651delinsGG
ENST00000688158.1:c.*1175_*1176delinsGG	ENSP00000509254.1:n.*1175_*1176delinsGG
ENST00000688308.1:c.1064_1065delinsGG	ENSP00000508752.1:p.Ser355Trp
ENST00000688922.1:c.985_986delinsGG
ENST00000693560.1:c.1583_1584delinsGG	ENSP00000509861.1:p.Ser528Trp
ENST00000371953.8:c.1064_1065delinsGG MANE Select	ENSP00000361021.3:p.Ser355Trp
ENST00000371953.7:c.1064_1065delinsGG	ENSP00000361021.3:p.Ser355Trp
NM_000314.5:c.1064_1065delinsGG	NP_000305.3:p.Ser355Trp
NM_000314.6:c.1064_1065delinsGG	NP_000305.3:p.Ser355Trp
NM_001304717.2:c.1583_1584delinsGG	NP_001291646.2:p.Ser528Trp
NM_001304718.1:c.473_474delinsGG	NP_001291647.1:p.Ser158Trp
XM_006717926.2:c.1019_1020delinsGG	XP_006717989.1:p.Ser340Trp
XM_011539982.1:c.968_969delinsGG	XP_011538284.1:p.Ser323Trp
XR_945791.1:n.1634_1635delinsGG
NM_000314.7:c.1064_1065delinsGG	NP_000305.3:p.Ser355Trp
NM_001304717.5:c.1583_1584delinsGG	NP_001291646.4:p.Ser528Trp
NM_001304718.2:c.473_474delinsGG	NP_001291647.1:p.Ser158Trp
NM_000314.8:c.1064_1065delinsGG MANE Select	NP_000305.3:p.Ser355Trp