Canonical Allele Identifier: CA891841591

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965350_87965352delinsATG , CM000672.2:g.87965350_87965352delinsATG	GRCh38
NC_000010.10:g.89725107_89725109delinsATG , CM000672.1:g.89725107_89725109delinsATG	GRCh37
NC_000010.9:g.89715087_89715089delinsATG	NCBI36
NG_007466.2:g.106912_106914delinsATG , LRG_311:g.106912_106914delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1183_1185delinsATG	ENSP00000514759.2:p.Ser395Met
ENST00000710265.1:c.*119_*121delinsATG	ENSP00000518161.1:n.*119_*121delinsATG
ENST00000688158.2:n.1825_1827delinsATG
ENST00000688922.2:c.*920_*922delinsATG	ENSP00000508742.2:n.*920_*922delinsATG
ENST00000700021.1:c.1045_1047delinsATG	ENSP00000514757.1:p.Ser349Met
ENST00000700022.1:c.*429_*431delinsATG	ENSP00000514758.1:n.*429_*431delinsATG
ENST00000700023.1:n.2248_2250delinsATG
ENST00000700024.1:n.2482_2484delinsATG
ENST00000706954.1:c.1090_1092delinsATG	ENSP00000516674.1:p.Ser364Met
ENST00000706955.1:c.*1125_*1127delinsATG	ENSP00000516675.1:n.*1125_*1127delinsATG
ENST00000686459.1:c.*676_*678delinsATG	ENSP00000508909.1:n.*676_*678delinsATG
ENST00000688158.1:c.*1201_*1203delinsATG	ENSP00000509254.1:n.*1201_*1203delinsATG
ENST00000688308.1:c.1090_1092delinsATG	ENSP00000508752.1:p.Ser364Met
ENST00000688922.1:c.1011_1013delinsATG
ENST00000693560.1:c.1609_1611delinsATG	ENSP00000509861.1:p.Ser537Met
ENST00000371953.8:c.1090_1092delinsATG MANE Select	ENSP00000361021.3:p.Ser364Met
ENST00000371953.7:c.1090_1092delinsATG	ENSP00000361021.3:p.Ser364Met
NM_000314.5:c.1090_1092delinsATG	NP_000305.3:p.Ser364Met
NM_000314.6:c.1090_1092delinsATG	NP_000305.3:p.Ser364Met
NM_001304717.2:c.1609_1611delinsATG	NP_001291646.2:p.Ser537Met
NM_001304718.1:c.499_501delinsATG	NP_001291647.1:p.Ser167Met
XM_006717926.2:c.1045_1047delinsATG	XP_006717989.1:p.Ser349Met
XM_011539982.1:c.994_996delinsATG	XP_011538284.1:p.Ser332Met
XR_945791.1:n.1660_1662delinsATG
NM_000314.7:c.1090_1092delinsATG	NP_000305.3:p.Ser364Met
NM_001304717.5:c.1609_1611delinsATG	NP_001291646.4:p.Ser537Met
NM_001304718.2:c.499_501delinsATG	NP_001291647.1:p.Ser167Met
NM_000314.8:c.1090_1092delinsATG MANE Select	NP_000305.3:p.Ser364Met