Canonical Allele Identifier: CA891841543

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965299_87965300delinsGG , CM000672.2:g.87965299_87965300delinsGG	GRCh38
NC_000010.10:g.89725056_89725057delinsGG , CM000672.1:g.89725056_89725057delinsGG	GRCh37
NC_000010.9:g.89715036_89715037delinsGG	NCBI36
NG_007466.2:g.106861_106862delinsGG , LRG_311:g.106861_106862delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1132_1133delinsGG	ENSP00000514759.2:p.Phe378Gly
ENST00000710265.1:c.*68_*69delinsGG	ENSP00000518161.1:n.*68_*69delinsGG
ENST00000688158.2:n.1774_1775delinsGG
ENST00000688922.2:c.*869_*870delinsGG	ENSP00000508742.2:n.*869_*870delinsGG
ENST00000700021.1:c.994_995delinsGG	ENSP00000514757.1:p.Phe332Gly
ENST00000700022.1:c.*378_*379delinsGG	ENSP00000514758.1:n.*378_*379delinsGG
ENST00000700023.1:n.2197_2198delinsGG
ENST00000700024.1:n.2431_2432delinsGG
ENST00000706954.1:c.1039_1040delinsGG	ENSP00000516674.1:p.Phe347Gly
ENST00000706955.1:c.*1074_*1075delinsGG	ENSP00000516675.1:n.*1074_*1075delinsGG
ENST00000686459.1:c.*625_*626delinsGG	ENSP00000508909.1:n.*625_*626delinsGG
ENST00000688158.1:c.*1150_*1151delinsGG	ENSP00000509254.1:n.*1150_*1151delinsGG
ENST00000688308.1:c.1039_1040delinsGG	ENSP00000508752.1:p.Phe347Gly
ENST00000688922.1:c.960_961delinsGG
ENST00000693560.1:c.1558_1559delinsGG	ENSP00000509861.1:p.Phe520Gly
ENST00000371953.8:c.1039_1040delinsGG MANE Select	ENSP00000361021.3:p.Phe347Gly
ENST00000371953.7:c.1039_1040delinsGG	ENSP00000361021.3:p.Phe347Gly
NM_000314.5:c.1039_1040delinsGG	NP_000305.3:p.Phe347Gly
NM_000314.6:c.1039_1040delinsGG	NP_000305.3:p.Phe347Gly
NM_001304717.2:c.1558_1559delinsGG	NP_001291646.2:p.Phe520Gly
NM_001304718.1:c.448_449delinsGG	NP_001291647.1:p.Phe150Gly
XM_006717926.2:c.994_995delinsGG	XP_006717989.1:p.Phe332Gly
XM_011539982.1:c.943_944delinsGG	XP_011538284.1:p.Phe315Gly
XR_945791.1:n.1609_1610delinsGG
NM_000314.7:c.1039_1040delinsGG	NP_000305.3:p.Phe347Gly
NM_001304717.5:c.1558_1559delinsGG	NP_001291646.4:p.Phe520Gly
NM_001304718.2:c.448_449delinsGG	NP_001291647.1:p.Phe150Gly
NM_000314.8:c.1039_1040delinsGG MANE Select	NP_000305.3:p.Phe347Gly