Canonical Allele Identifier: CA891839195

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952235_87952237delinsATG , CM000672.2:g.87952235_87952237delinsATG	GRCh38
NC_000010.10:g.89711992_89711994delinsATG , CM000672.1:g.89711992_89711994delinsATG	GRCh37
NC_000010.9:g.89701972_89701974delinsATG	NCBI36
NG_007466.2:g.93797_93799delinsATG , LRG_311:g.93797_93799delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.610_612delinsATG	ENSP00000514759.2:p.Pro204Met
ENST00000710265.1:c.610_612delinsATG	ENSP00000518161.1:p.Pro204Met
ENST00000472832.3:c.610_612delinsATG	ENSP00000483066.2:p.Pro204Met
ENST00000688158.2:n.1345_1347delinsATG
ENST00000688922.2:c.*440_*442delinsATG	ENSP00000508742.2:n.*440_*442delinsATG
ENST00000700021.1:c.565_567delinsATG	ENSP00000514757.1:p.Pro189Met
ENST00000700022.1:c.493-5618_493-5616delinsATG	ENSP00000514758.1:n.493-5618_493-5616delinsATG
ENST00000700023.1:n.1768_1770delinsATG
ENST00000700024.1:n.2002_2004delinsATG
ENST00000700025.1:n.1379_1381delinsATG
ENST00000700029.1:c.444_446delinsATG
ENST00000706954.1:c.610_612delinsATG	ENSP00000516674.1:p.Pro204Met
ENST00000706955.1:c.*645_*647delinsATG	ENSP00000516675.1:n.*645_*647delinsATG
ENST00000686459.1:c.*196_*198delinsATG	ENSP00000508909.1:n.*196_*198delinsATG
ENST00000688158.1:c.*721_*723delinsATG	ENSP00000509254.1:n.*721_*723delinsATG
ENST00000688308.1:c.610_612delinsATG	ENSP00000508752.1:p.Pro204Met
ENST00000688922.1:c.531_533delinsATG
ENST00000693560.1:c.1129_1131delinsATG	ENSP00000509861.1:p.Pro377Met
ENST00000371953.8:c.610_612delinsATG MANE Select	ENSP00000361021.3:p.Pro204Met
ENST00000371953.7:c.610_612delinsATG	ENSP00000361021.3:p.Pro204Met
ENST00000472832.2:c.37_39delinsATG	ENSP00000483066.1:p.Pro13Met
NM_000314.5:c.610_612delinsATG	NP_000305.3:p.Pro204Met
NM_000314.6:c.610_612delinsATG	NP_000305.3:p.Pro204Met
NM_001304717.2:c.1129_1131delinsATG	NP_001291646.2:p.Pro377Met
NM_001304718.1:c.19_21delinsATG	NP_001291647.1:p.Pro7Met
XM_006717926.2:c.565_567delinsATG	XP_006717989.1:p.Pro189Met
XM_011539981.1:c.610_612delinsATG	XP_011538283.1:p.Pro204Met
XM_011539982.1:c.514_516delinsATG	XP_011538284.1:p.Pro172Met
XR_945791.1:n.1205-5618_1205-5616delinsATG
NM_000314.7:c.610_612delinsATG	NP_000305.3:p.Pro204Met
NM_001304717.5:c.1129_1131delinsATG	NP_001291646.4:p.Pro377Met
NM_001304718.2:c.19_21delinsATG	NP_001291647.1:p.Pro7Met
NM_000314.8:c.610_612delinsATG MANE Select	NP_000305.3:p.Pro204Met