Canonical Allele Identifier: CA891841092

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960951_87960952delinsCG , CM000672.2:g.87960951_87960952delinsCG	GRCh38
NC_000010.10:g.89720708_89720709delinsCG , CM000672.1:g.89720708_89720709delinsCG	GRCh37
NC_000010.9:g.89710688_89710689delinsCG	NCBI36
NG_007466.2:g.102513_102514delinsCG , LRG_311:g.102513_102514delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.952_953delinsCG	ENSP00000514759.2:p.Ser318Arg
ENST00000710265.1:c.859_860delinsCG	ENSP00000518161.1:p.Ser287Arg
ENST00000472832.3:c.859_860delinsCG	ENSP00000483066.2:p.Ser287Arg
ENST00000688158.2:n.1594_1595delinsCG
ENST00000688922.2:c.*689_*690delinsCG	ENSP00000508742.2:n.*689_*690delinsCG
ENST00000700021.1:c.814_815delinsCG	ENSP00000514757.1:p.Ser272Arg
ENST00000700022.1:c.*198_*199delinsCG	ENSP00000514758.1:n.*198_*199delinsCG
ENST00000700023.1:n.2017_2018delinsCG
ENST00000700024.1:n.2251_2252delinsCG
ENST00000700025.1:n.1628_1629delinsCG
ENST00000700026.1:n.496_497delinsCG
ENST00000700029.1:c.786_787delinsCG
ENST00000706954.1:c.859_860delinsCG	ENSP00000516674.1:p.Ser287Arg
ENST00000706955.1:c.*894_*895delinsCG	ENSP00000516675.1:n.*894_*895delinsCG
ENST00000686459.1:c.*445_*446delinsCG	ENSP00000508909.1:n.*445_*446delinsCG
ENST00000688158.1:c.*970_*971delinsCG	ENSP00000509254.1:n.*970_*971delinsCG
ENST00000688308.1:c.859_860delinsCG	ENSP00000508752.1:p.Ser287Arg
ENST00000688922.1:c.780_781delinsCG
ENST00000693560.1:c.1378_1379delinsCG	ENSP00000509861.1:p.Ser460Arg
ENST00000371953.8:c.859_860delinsCG MANE Select	ENSP00000361021.3:p.Ser287Arg
ENST00000371953.7:c.859_860delinsCG	ENSP00000361021.3:p.Ser287Arg
ENST00000472832.2:c.286_287delinsCG	ENSP00000483066.1:p.Ser96Arg
NM_000314.5:c.859_860delinsCG	NP_000305.3:p.Ser287Arg
NM_000314.6:c.859_860delinsCG	NP_000305.3:p.Ser287Arg
NM_001304717.2:c.1378_1379delinsCG	NP_001291646.2:p.Ser460Arg
NM_001304718.1:c.268_269delinsCG	NP_001291647.1:p.Ser90Arg
XM_006717926.2:c.814_815delinsCG	XP_006717989.1:p.Ser272Arg
XM_011539981.1:c.859_860delinsCG	XP_011538283.1:p.Ser287Arg
XM_011539982.1:c.763_764delinsCG	XP_011538284.1:p.Ser255Arg
XR_945791.1:n.1429_1430delinsCG
NM_000314.7:c.859_860delinsCG	NP_000305.3:p.Ser287Arg
NM_001304717.5:c.1378_1379delinsCG	NP_001291646.4:p.Ser460Arg
NM_001304718.2:c.268_269delinsCG	NP_001291647.1:p.Ser90Arg
NM_000314.8:c.859_860delinsCG MANE Select	NP_000305.3:p.Ser287Arg