Canonical Allele Identifier: CA891835082

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960953delinsATG , CM000672.2:g.87960951_87960953delinsATG	GRCh38
NC_000010.10:g.89720708_89720710delinsATG , CM000672.1:g.89720708_89720710delinsATG	GRCh37
NC_000010.9:g.89710688_89710690delinsATG	NCBI36
NG_007466.2:g.102513_102515delinsATG , LRG_311:g.102513_102515delinsATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.952_954delinsATG	ENSP00000514759.2:p.Ser318Met
ENST00000710265.1:c.859_861delinsATG	ENSP00000518161.1:p.Ser287Met
ENST00000472832.3:c.859_861delinsATG	ENSP00000483066.2:p.Ser287Met
ENST00000688158.2:n.1594_1596delinsATG
ENST00000688922.2:c.*689_*691delinsATG	ENSP00000508742.2:n.*689_*691delinsATG
ENST00000700021.1:c.814_816delinsATG	ENSP00000514757.1:p.Ser272Met
ENST00000700022.1:c.*198_*200delinsATG	ENSP00000514758.1:n.*198_*200delinsATG
ENST00000700023.1:n.2017_2019delinsATG
ENST00000700024.1:n.2251_2253delinsATG
ENST00000700025.1:n.1628_1630delinsATG
ENST00000700026.1:n.496_498delinsATG
ENST00000700029.1:c.786_788delinsATG
ENST00000706954.1:c.859_861delinsATG	ENSP00000516674.1:p.Ser287Met
ENST00000706955.1:c.*894_*896delinsATG	ENSP00000516675.1:n.*894_*896delinsATG
ENST00000686459.1:c.*445_*447delinsATG	ENSP00000508909.1:n.*445_*447delinsATG
ENST00000688158.1:c.*970_*972delinsATG	ENSP00000509254.1:n.*970_*972delinsATG
ENST00000688308.1:c.859_861delinsATG	ENSP00000508752.1:p.Ser287Met
ENST00000688922.1:c.780_782delinsATG
ENST00000693560.1:c.1378_1380delinsATG	ENSP00000509861.1:p.Ser460Met
ENST00000371953.8:c.859_861delinsATG MANE Select	ENSP00000361021.3:p.Ser287Met
ENST00000371953.7:c.859_861delinsATG	ENSP00000361021.3:p.Ser287Met
ENST00000472832.2:c.286_288delinsATG	ENSP00000483066.1:p.Ser96Met
NM_000314.5:c.859_861delinsATG	NP_000305.3:p.Ser287Met
NM_000314.6:c.859_861delinsATG	NP_000305.3:p.Ser287Met
NM_001304717.2:c.1378_1380delinsATG	NP_001291646.2:p.Ser460Met
NM_001304718.1:c.268_270delinsATG	NP_001291647.1:p.Ser90Met
XM_006717926.2:c.814_816delinsATG	XP_006717989.1:p.Ser272Met
XM_011539981.1:c.859_861delinsATG	XP_011538283.1:p.Ser287Met
XM_011539982.1:c.763_765delinsATG	XP_011538284.1:p.Ser255Met
XR_945791.1:n.1429_1431delinsATG
NM_000314.7:c.859_861delinsATG	NP_000305.3:p.Ser287Met
NM_001304717.5:c.1378_1380delinsATG	NP_001291646.4:p.Ser460Met
NM_001304718.2:c.268_270delinsATG	NP_001291647.1:p.Ser90Met
NM_000314.8:c.859_861delinsATG MANE Select	NP_000305.3:p.Ser287Met