Canonical Allele Identifier: CA891841545

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965299_87965300delinsGC , CM000672.2:g.87965299_87965300delinsGC	GRCh38
NC_000010.10:g.89725056_89725057delinsGC , CM000672.1:g.89725056_89725057delinsGC	GRCh37
NC_000010.9:g.89715036_89715037delinsGC	NCBI36
NG_007466.2:g.106861_106862delinsGC , LRG_311:g.106861_106862delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1132_1133delinsGC	ENSP00000514759.2:p.Phe378Ala
ENST00000710265.1:c.*68_*69delinsGC	ENSP00000518161.1:n.*68_*69delinsGC
ENST00000688158.2:n.1774_1775delinsGC
ENST00000688922.2:c.*869_*870delinsGC	ENSP00000508742.2:n.*869_*870delinsGC
ENST00000700021.1:c.994_995delinsGC	ENSP00000514757.1:p.Phe332Ala
ENST00000700022.1:c.*378_*379delinsGC	ENSP00000514758.1:n.*378_*379delinsGC
ENST00000700023.1:n.2197_2198delinsGC
ENST00000700024.1:n.2431_2432delinsGC
ENST00000706954.1:c.1039_1040delinsGC	ENSP00000516674.1:p.Phe347Ala
ENST00000706955.1:c.*1074_*1075delinsGC	ENSP00000516675.1:n.*1074_*1075delinsGC
ENST00000686459.1:c.*625_*626delinsGC	ENSP00000508909.1:n.*625_*626delinsGC
ENST00000688158.1:c.*1150_*1151delinsGC	ENSP00000509254.1:n.*1150_*1151delinsGC
ENST00000688308.1:c.1039_1040delinsGC	ENSP00000508752.1:p.Phe347Ala
ENST00000688922.1:c.960_961delinsGC
ENST00000693560.1:c.1558_1559delinsGC	ENSP00000509861.1:p.Phe520Ala
ENST00000371953.8:c.1039_1040delinsGC MANE Select	ENSP00000361021.3:p.Phe347Ala
ENST00000371953.7:c.1039_1040delinsGC	ENSP00000361021.3:p.Phe347Ala
NM_000314.5:c.1039_1040delinsGC	NP_000305.3:p.Phe347Ala
NM_000314.6:c.1039_1040delinsGC	NP_000305.3:p.Phe347Ala
NM_001304717.2:c.1558_1559delinsGC	NP_001291646.2:p.Phe520Ala
NM_001304718.1:c.448_449delinsGC	NP_001291647.1:p.Phe150Ala
XM_006717926.2:c.994_995delinsGC	XP_006717989.1:p.Phe332Ala
XM_011539982.1:c.943_944delinsGC	XP_011538284.1:p.Phe315Ala
XR_945791.1:n.1609_1610delinsGC
NM_000314.7:c.1039_1040delinsGC	NP_000305.3:p.Phe347Ala
NM_001304717.5:c.1558_1559delinsGC	NP_001291646.4:p.Phe520Ala
NM_001304718.2:c.448_449delinsGC	NP_001291647.1:p.Phe150Ala
NM_000314.8:c.1039_1040delinsGC MANE Select	NP_000305.3:p.Phe347Ala