Canonical Allele Identifier: CA891836942

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961101_87961103delinsATG , CM000672.2:g.87961101_87961103delinsATG	GRCh38
NC_000010.10:g.89720858_89720860delinsATG , CM000672.1:g.89720858_89720860delinsATG	GRCh37
NC_000010.9:g.89710838_89710840delinsATG	NCBI36
NG_007466.2:g.102663_102665delinsATG , LRG_311:g.102663_102665delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1102_1104delinsATG	ENSP00000514759.2:p.Phe368Met
ENST00000710265.1:c.1009_1011delinsATG	ENSP00000518161.1:p.Phe337Met
ENST00000472832.3:c.1009_1011delinsATG	ENSP00000483066.2:p.Phe337Met
ENST00000688158.2:n.1744_1746delinsATG
ENST00000688922.2:c.*839_*841delinsATG	ENSP00000508742.2:n.*839_*841delinsATG
ENST00000700021.1:c.964_966delinsATG	ENSP00000514757.1:p.Phe322Met
ENST00000700022.1:c.*348_*350delinsATG	ENSP00000514758.1:n.*348_*350delinsATG
ENST00000700023.1:n.2167_2169delinsATG
ENST00000700024.1:n.2401_2403delinsATG
ENST00000700025.1:n.1778_1780delinsATG
ENST00000700026.1:n.646_648delinsATG
ENST00000706954.1:c.1009_1011delinsATG	ENSP00000516674.1:p.Phe337Met
ENST00000706955.1:c.*1044_*1046delinsATG	ENSP00000516675.1:n.*1044_*1046delinsATG
ENST00000686459.1:c.*595_*597delinsATG	ENSP00000508909.1:n.*595_*597delinsATG
ENST00000688158.1:c.*1120_*1122delinsATG	ENSP00000509254.1:n.*1120_*1122delinsATG
ENST00000688308.1:c.1009_1011delinsATG	ENSP00000508752.1:p.Phe337Met
ENST00000688922.1:c.930_932delinsATG
ENST00000693560.1:c.1528_1530delinsATG	ENSP00000509861.1:p.Phe510Met
ENST00000371953.8:c.1009_1011delinsATG MANE Select	ENSP00000361021.3:p.Phe337Met
ENST00000371953.7:c.1009_1011delinsATG	ENSP00000361021.3:p.Phe337Met
ENST00000472832.2:c.436_438delinsATG	ENSP00000483066.1:p.Phe146Met
NM_000314.5:c.1009_1011delinsATG	NP_000305.3:p.Phe337Met
NM_000314.6:c.1009_1011delinsATG	NP_000305.3:p.Phe337Met
NM_001304717.2:c.1528_1530delinsATG	NP_001291646.2:p.Phe510Met
NM_001304718.1:c.418_420delinsATG	NP_001291647.1:p.Phe140Met
XM_006717926.2:c.964_966delinsATG	XP_006717989.1:p.Phe322Met
XM_011539981.1:c.1009_1011delinsATG	XP_011538283.1:p.Phe337Met
XM_011539982.1:c.913_915delinsATG	XP_011538284.1:p.Phe305Met
XR_945791.1:n.1579_1581delinsATG
NM_000314.7:c.1009_1011delinsATG	NP_000305.3:p.Phe337Met
NM_001304717.5:c.1528_1530delinsATG	NP_001291646.4:p.Phe510Met
NM_001304718.2:c.418_420delinsATG	NP_001291647.1:p.Phe140Met
NM_000314.8:c.1009_1011delinsATG MANE Select	NP_000305.3:p.Phe337Met