Canonical Allele Identifier: CA891838103

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965435_87965436delinsGG , CM000672.2:g.87965435_87965436delinsGG	GRCh38
NC_000010.10:g.89725192_89725193delinsGG , CM000672.1:g.89725192_89725193delinsGG	GRCh37
NC_000010.9:g.89715172_89715173delinsGG	NCBI36
NG_007466.2:g.106997_106998delinsGG , LRG_311:g.106997_106998delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1268_1269delinsGG	ENSP00000514759.2:p.Phe423Trp
ENST00000710265.1:c.*204_*205delinsGG	ENSP00000518161.1:n.*204_*205delinsGG
ENST00000688158.2:n.1910_1911delinsGG
ENST00000688922.2:c.*1005_*1006delinsGG	ENSP00000508742.2:n.*1005_*1006delinsGG
ENST00000700021.1:c.1130_1131delinsGG	ENSP00000514757.1:p.Phe377Trp
ENST00000700022.1:c.*514_*515delinsGG	ENSP00000514758.1:n.*514_*515delinsGG
ENST00000700023.1:n.2333_2334delinsGG
ENST00000700024.1:n.2567_2568delinsGG
ENST00000706954.1:c.1175_1176delinsGG	ENSP00000516674.1:p.Phe392Trp
ENST00000706955.1:c.*1210_*1211delinsGG	ENSP00000516675.1:n.*1210_*1211delinsGG
ENST00000686459.1:c.*761_*762delinsGG	ENSP00000508909.1:n.*761_*762delinsGG
ENST00000688158.1:c.*1286_*1287delinsGG	ENSP00000509254.1:n.*1286_*1287delinsGG
ENST00000688308.1:c.1175_1176delinsGG	ENSP00000508752.1:p.Phe392Trp
ENST00000688922.1:c.1096_1097delinsGG
ENST00000693560.1:c.1694_1695delinsGG	ENSP00000509861.1:p.Phe565Trp
ENST00000371953.8:c.1175_1176delinsGG MANE Select	ENSP00000361021.3:p.Phe392Trp
ENST00000371953.7:c.1175_1176delinsGG	ENSP00000361021.3:p.Phe392Trp
NM_000314.5:c.1175_1176delinsGG	NP_000305.3:p.Phe392Trp
NM_000314.6:c.1175_1176delinsGG	NP_000305.3:p.Phe392Trp
NM_001304717.2:c.1694_1695delinsGG	NP_001291646.2:p.Phe565Trp
NM_001304718.1:c.584_585delinsGG	NP_001291647.1:p.Phe195Trp
XM_006717926.2:c.1130_1131delinsGG	XP_006717989.1:p.Phe377Trp
XM_011539982.1:c.1079_1080delinsGG	XP_011538284.1:p.Phe360Trp
XR_945791.1:n.1745_1746delinsGG
NM_000314.7:c.1175_1176delinsGG	NP_000305.3:p.Phe392Trp
NM_001304717.5:c.1694_1695delinsGG	NP_001291646.4:p.Phe565Trp
NM_001304718.2:c.584_585delinsGG	NP_001291647.1:p.Phe195Trp
NM_000314.8:c.1175_1176delinsGG MANE Select	NP_000305.3:p.Phe392Trp