Canonical Allele Identifier: CA891841091

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960952delinsCA , CM000672.2:g.87960951_87960952delinsCA	GRCh38
NC_000010.10:g.89720708_89720709delinsCA , CM000672.1:g.89720708_89720709delinsCA	GRCh37
NC_000010.9:g.89710688_89710689delinsCA	NCBI36
NG_007466.2:g.102513_102514delinsCA , LRG_311:g.102513_102514delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.952_953delinsCA	ENSP00000514759.2:p.Ser318Gln
ENST00000710265.1:c.859_860delinsCA	ENSP00000518161.1:p.Ser287Gln
ENST00000472832.3:c.859_860delinsCA	ENSP00000483066.2:p.Ser287Gln
ENST00000688158.2:n.1594_1595delinsCA
ENST00000688922.2:c.*689_*690delinsCA	ENSP00000508742.2:n.*689_*690delinsCA
ENST00000700021.1:c.814_815delinsCA	ENSP00000514757.1:p.Ser272Gln
ENST00000700022.1:c.*198_*199delinsCA	ENSP00000514758.1:n.*198_*199delinsCA
ENST00000700023.1:n.2017_2018delinsCA
ENST00000700024.1:n.2251_2252delinsCA
ENST00000700025.1:n.1628_1629delinsCA
ENST00000700026.1:n.496_497delinsCA
ENST00000700029.1:c.786_787delinsCA
ENST00000706954.1:c.859_860delinsCA	ENSP00000516674.1:p.Ser287Gln
ENST00000706955.1:c.*894_*895delinsCA	ENSP00000516675.1:n.*894_*895delinsCA
ENST00000686459.1:c.*445_*446delinsCA	ENSP00000508909.1:n.*445_*446delinsCA
ENST00000688158.1:c.*970_*971delinsCA	ENSP00000509254.1:n.*970_*971delinsCA
ENST00000688308.1:c.859_860delinsCA	ENSP00000508752.1:p.Ser287Gln
ENST00000688922.1:c.780_781delinsCA
ENST00000693560.1:c.1378_1379delinsCA	ENSP00000509861.1:p.Ser460Gln
ENST00000371953.8:c.859_860delinsCA MANE Select	ENSP00000361021.3:p.Ser287Gln
ENST00000371953.7:c.859_860delinsCA	ENSP00000361021.3:p.Ser287Gln
ENST00000472832.2:c.286_287delinsCA	ENSP00000483066.1:p.Ser96Gln
NM_000314.5:c.859_860delinsCA	NP_000305.3:p.Ser287Gln
NM_000314.6:c.859_860delinsCA	NP_000305.3:p.Ser287Gln
NM_001304717.2:c.1378_1379delinsCA	NP_001291646.2:p.Ser460Gln
NM_001304718.1:c.268_269delinsCA	NP_001291647.1:p.Ser90Gln
XM_006717926.2:c.814_815delinsCA	XP_006717989.1:p.Ser272Gln
XM_011539981.1:c.859_860delinsCA	XP_011538283.1:p.Ser287Gln
XM_011539982.1:c.763_764delinsCA	XP_011538284.1:p.Ser255Gln
XR_945791.1:n.1429_1430delinsCA
NM_000314.7:c.859_860delinsCA	NP_000305.3:p.Ser287Gln
NM_001304717.5:c.1378_1379delinsCA	NP_001291646.4:p.Ser460Gln
NM_001304718.2:c.268_269delinsCA	NP_001291647.1:p.Ser90Gln
NM_000314.8:c.859_860delinsCA MANE Select	NP_000305.3:p.Ser287Gln