Canonical Allele Identifier: CA891840203

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960904_87960905delinsGG , CM000672.2:g.87960904_87960905delinsGG	GRCh38
NC_000010.10:g.89720661_89720662delinsGG , CM000672.1:g.89720661_89720662delinsGG	GRCh37
NC_000010.9:g.89710641_89710642delinsGG	NCBI36
NG_007466.2:g.102466_102467delinsGG , LRG_311:g.102466_102467delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.905_906delinsGG	ENSP00000514759.2:p.Phe302Trp
ENST00000710265.1:c.812_813delinsGG	ENSP00000518161.1:p.Phe271Trp
ENST00000472832.3:c.812_813delinsGG	ENSP00000483066.2:p.Phe271Trp
ENST00000688158.2:n.1547_1548delinsGG
ENST00000688922.2:c.*642_*643delinsGG	ENSP00000508742.2:n.*642_*643delinsGG
ENST00000700021.1:c.767_768delinsGG	ENSP00000514757.1:p.Phe256Trp
ENST00000700022.1:c.*151_*152delinsGG	ENSP00000514758.1:n.*151_*152delinsGG
ENST00000700023.1:n.1970_1971delinsGG
ENST00000700024.1:n.2204_2205delinsGG
ENST00000700025.1:n.1581_1582delinsGG
ENST00000700026.1:n.449_450delinsGG
ENST00000700029.1:c.739_740delinsGG
ENST00000706954.1:c.812_813delinsGG	ENSP00000516674.1:p.Phe271Trp
ENST00000706955.1:c.*847_*848delinsGG	ENSP00000516675.1:n.*847_*848delinsGG
ENST00000686459.1:c.*398_*399delinsGG	ENSP00000508909.1:n.*398_*399delinsGG
ENST00000688158.1:c.*923_*924delinsGG	ENSP00000509254.1:n.*923_*924delinsGG
ENST00000688308.1:c.812_813delinsGG	ENSP00000508752.1:p.Phe271Trp
ENST00000688922.1:c.733_734delinsGG
ENST00000693560.1:c.1331_1332delinsGG	ENSP00000509861.1:p.Phe444Trp
ENST00000371953.8:c.812_813delinsGG MANE Select	ENSP00000361021.3:p.Phe271Trp
ENST00000371953.7:c.812_813delinsGG	ENSP00000361021.3:p.Phe271Trp
ENST00000472832.2:c.239_240delinsGG	ENSP00000483066.1:p.Phe80Trp
NM_000314.5:c.812_813delinsGG	NP_000305.3:p.Phe271Trp
NM_000314.6:c.812_813delinsGG	NP_000305.3:p.Phe271Trp
NM_001304717.2:c.1331_1332delinsGG	NP_001291646.2:p.Phe444Trp
NM_001304718.1:c.221_222delinsGG	NP_001291647.1:p.Phe74Trp
XM_006717926.2:c.767_768delinsGG	XP_006717989.1:p.Phe256Trp
XM_011539981.1:c.812_813delinsGG	XP_011538283.1:p.Phe271Trp
XM_011539982.1:c.716_717delinsGG	XP_011538284.1:p.Phe239Trp
XR_945791.1:n.1382_1383delinsGG
NM_000314.7:c.812_813delinsGG	NP_000305.3:p.Phe271Trp
NM_001304717.5:c.1331_1332delinsGG	NP_001291646.4:p.Phe444Trp
NM_001304718.2:c.221_222delinsGG	NP_001291647.1:p.Phe74Trp
NM_000314.8:c.812_813delinsGG MANE Select	NP_000305.3:p.Phe271Trp