Canonical Allele Identifier: CA891838143

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965443_87965445delinsATG , CM000672.2:g.87965443_87965445delinsATG	GRCh38
NC_000010.10:g.89725200_89725202delinsATG , CM000672.1:g.89725200_89725202delinsATG	GRCh37
NC_000010.9:g.89715180_89715182delinsATG	NCBI36
NG_007466.2:g.107005_107007delinsATG , LRG_311:g.107005_107007delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1276_1278delinsATG	ENSP00000514759.2:p.Asp426Met
ENST00000710265.1:c.*212_*214delinsATG	ENSP00000518161.1:n.*212_*214delinsATG
ENST00000688158.2:n.1918_1920delinsATG
ENST00000688922.2:c.*1013_*1015delinsATG	ENSP00000508742.2:n.*1013_*1015delinsATG
ENST00000700021.1:c.1138_1140delinsATG	ENSP00000514757.1:p.Asp380Met
ENST00000700022.1:c.*522_*524delinsATG	ENSP00000514758.1:n.*522_*524delinsATG
ENST00000700023.1:n.2341_2343delinsATG
ENST00000700024.1:n.2575_2577delinsATG
ENST00000706954.1:c.1183_1185delinsATG	ENSP00000516674.1:p.Asp395Met
ENST00000706955.1:c.*1218_*1220delinsATG	ENSP00000516675.1:n.*1218_*1220delinsATG
ENST00000686459.1:c.*769_*771delinsATG	ENSP00000508909.1:n.*769_*771delinsATG
ENST00000688158.1:c.*1294_*1296delinsATG	ENSP00000509254.1:n.*1294_*1296delinsATG
ENST00000688308.1:c.1183_1185delinsATG	ENSP00000508752.1:p.Asp395Met
ENST00000688922.1:c.1104_1106delinsATG
ENST00000693560.1:c.1702_1704delinsATG	ENSP00000509861.1:p.Asp568Met
ENST00000371953.8:c.1183_1185delinsATG MANE Select	ENSP00000361021.3:p.Asp395Met
ENST00000371953.7:c.1183_1185delinsATG	ENSP00000361021.3:p.Asp395Met
NM_000314.5:c.1183_1185delinsATG	NP_000305.3:p.Asp395Met
NM_000314.6:c.1183_1185delinsATG	NP_000305.3:p.Asp395Met
NM_001304717.2:c.1702_1704delinsATG	NP_001291646.2:p.Asp568Met
NM_001304718.1:c.592_594delinsATG	NP_001291647.1:p.Asp198Met
XM_006717926.2:c.1138_1140delinsATG	XP_006717989.1:p.Asp380Met
XM_011539982.1:c.1087_1089delinsATG	XP_011538284.1:p.Asp363Met
XR_945791.1:n.1753_1755delinsATG
NM_000314.7:c.1183_1185delinsATG	NP_000305.3:p.Asp395Met
NM_001304717.5:c.1702_1704delinsATG	NP_001291646.4:p.Asp568Met
NM_001304718.2:c.592_594delinsATG	NP_001291647.1:p.Asp198Met
NM_000314.8:c.1183_1185delinsATG MANE Select	NP_000305.3:p.Asp395Met