Canonical Allele Identifier: CA891841567

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965323_87965324delinsCG , CM000672.2:g.87965323_87965324delinsCG	GRCh38
NC_000010.10:g.89725080_89725081delinsCG , CM000672.1:g.89725080_89725081delinsCG	GRCh37
NC_000010.9:g.89715060_89715061delinsCG	NCBI36
NG_007466.2:g.106885_106886delinsCG , LRG_311:g.106885_106886delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1156_1157delinsCG	ENSP00000514759.2:p.Ser386Arg
ENST00000710265.1:c.*92_*93delinsCG	ENSP00000518161.1:n.*92_*93delinsCG
ENST00000688158.2:n.1798_1799delinsCG
ENST00000688922.2:c.*893_*894delinsCG	ENSP00000508742.2:n.*893_*894delinsCG
ENST00000700021.1:c.1018_1019delinsCG	ENSP00000514757.1:p.Ser340Arg
ENST00000700022.1:c.*402_*403delinsCG	ENSP00000514758.1:n.*402_*403delinsCG
ENST00000700023.1:n.2221_2222delinsCG
ENST00000700024.1:n.2455_2456delinsCG
ENST00000706954.1:c.1063_1064delinsCG	ENSP00000516674.1:p.Ser355Arg
ENST00000706955.1:c.*1098_*1099delinsCG	ENSP00000516675.1:n.*1098_*1099delinsCG
ENST00000686459.1:c.*649_*650delinsCG	ENSP00000508909.1:n.*649_*650delinsCG
ENST00000688158.1:c.*1174_*1175delinsCG	ENSP00000509254.1:n.*1174_*1175delinsCG
ENST00000688308.1:c.1063_1064delinsCG	ENSP00000508752.1:p.Ser355Arg
ENST00000688922.1:c.984_985delinsCG
ENST00000693560.1:c.1582_1583delinsCG	ENSP00000509861.1:p.Ser528Arg
ENST00000371953.8:c.1063_1064delinsCG MANE Select	ENSP00000361021.3:p.Ser355Arg
ENST00000371953.7:c.1063_1064delinsCG	ENSP00000361021.3:p.Ser355Arg
NM_000314.5:c.1063_1064delinsCG	NP_000305.3:p.Ser355Arg
NM_000314.6:c.1063_1064delinsCG	NP_000305.3:p.Ser355Arg
NM_001304717.2:c.1582_1583delinsCG	NP_001291646.2:p.Ser528Arg
NM_001304718.1:c.472_473delinsCG	NP_001291647.1:p.Ser158Arg
XM_006717926.2:c.1018_1019delinsCG	XP_006717989.1:p.Ser340Arg
XM_011539982.1:c.967_968delinsCG	XP_011538284.1:p.Ser323Arg
XR_945791.1:n.1633_1634delinsCG
NM_000314.7:c.1063_1064delinsCG	NP_000305.3:p.Ser355Arg
NM_001304717.5:c.1582_1583delinsCG	NP_001291646.4:p.Ser528Arg
NM_001304718.2:c.472_473delinsCG	NP_001291647.1:p.Ser158Arg
NM_000314.8:c.1063_1064delinsCG MANE Select	NP_000305.3:p.Ser355Arg