Canonical Allele Identifier: CA891839826

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957954_87957955delinsTT , CM000672.2:g.87957954_87957955delinsTT	GRCh38
NC_000010.10:g.89717711_89717712delinsTT , CM000672.1:g.89717711_89717712delinsTT	GRCh37
NC_000010.9:g.89707691_89707692delinsTT	NCBI36
NG_007466.2:g.99516_99517delinsTT , LRG_311:g.99516_99517delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.736_737delinsTT	ENSP00000514759.2:p.Pro246Leu
ENST00000710265.1:c.736_737delinsTT	ENSP00000518161.1:p.Pro246Leu
ENST00000472832.3:c.736_737delinsTT	ENSP00000483066.2:p.Pro246Leu
ENST00000688158.2:n.1471_1472delinsTT
ENST00000688922.2:c.*566_*567delinsTT	ENSP00000508742.2:n.*566_*567delinsTT
ENST00000700021.1:c.691_692delinsTT	ENSP00000514757.1:p.Pro231Leu
ENST00000700022.1:c.*75_*76delinsTT	ENSP00000514758.1:n.*75_*76delinsTT
ENST00000700023.1:n.1894_1895delinsTT
ENST00000700024.1:n.2128_2129delinsTT
ENST00000700025.1:n.1505_1506delinsTT
ENST00000700026.1:n.373_374delinsTT
ENST00000700029.1:c.570_571delinsTT
ENST00000706954.1:c.736_737delinsTT	ENSP00000516674.1:p.Pro246Leu
ENST00000706955.1:c.*771_*772delinsTT	ENSP00000516675.1:n.*771_*772delinsTT
ENST00000686459.1:c.*322_*323delinsTT	ENSP00000508909.1:n.*322_*323delinsTT
ENST00000688158.1:c.*847_*848delinsTT	ENSP00000509254.1:n.*847_*848delinsTT
ENST00000688308.1:c.736_737delinsTT	ENSP00000508752.1:p.Pro246Leu
ENST00000688922.1:c.657_658delinsTT
ENST00000693560.1:c.1255_1256delinsTT	ENSP00000509861.1:p.Pro419Leu
ENST00000371953.8:c.736_737delinsTT MANE Select	ENSP00000361021.3:p.Pro246Leu
ENST00000371953.7:c.736_737delinsTT	ENSP00000361021.3:p.Pro246Leu
ENST00000472832.2:c.163_164delinsTT	ENSP00000483066.1:p.Pro55Leu
NM_000314.5:c.736_737delinsTT	NP_000305.3:p.Pro246Leu
NM_000314.6:c.736_737delinsTT	NP_000305.3:p.Pro246Leu
NM_001304717.2:c.1255_1256delinsTT	NP_001291646.2:p.Pro419Leu
NM_001304718.1:c.145_146delinsTT	NP_001291647.1:p.Pro49Leu
XM_006717926.2:c.691_692delinsTT	XP_006717989.1:p.Pro231Leu
XM_011539981.1:c.736_737delinsTT	XP_011538283.1:p.Pro246Leu
XM_011539982.1:c.640_641delinsTT	XP_011538284.1:p.Pro214Leu
XR_945791.1:n.1306_1307delinsTT
NM_000314.7:c.736_737delinsTT	NP_000305.3:p.Pro246Leu
NM_001304717.5:c.1255_1256delinsTT	NP_001291646.4:p.Pro419Leu
NM_001304718.2:c.145_146delinsTT	NP_001291647.1:p.Pro49Leu
NM_000314.8:c.736_737delinsTT MANE Select	NP_000305.3:p.Pro246Leu