Canonical Allele Identifier: CA891836434

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933034_87933035delinsTT , CM000672.2:g.87933034_87933035delinsTT	GRCh38
NC_000010.10:g.89692791_89692792delinsTT , CM000672.1:g.89692791_89692792delinsTT	GRCh37
NC_000010.9:g.89682771_89682772delinsTT	NCBI36
NG_007466.2:g.74596_74597delinsTT , LRG_311:g.74596_74597delinsTT

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.275_276delinsTT MANE Select	NP_000305.3:p.Asp92Val
ENST00000371953.8:c.275_276delinsTT MANE Select	ENSP00000361021.3:p.Asp92Val
NM_000314.5:c.275_276delinsTT	NP_000305.3:p.Asp92Val
NM_000314.6:c.275_276delinsTT	NP_000305.3:p.Asp92Val
NM_000314.7:c.275_276delinsTT	NP_000305.3:p.Asp92Val
NM_001304717.2:c.794_795delinsTT	NP_001291646.2:p.Asp265Val
NM_001304717.5:c.794_795delinsTT	NP_001291646.4:p.Asp265Val
NM_001304718.1:c.-476_-475delinsTT	NP_001291647.1:n.-476_-475delinsTT
NM_001304718.2:c.-476_-475delinsTT	NP_001291647.1:n.-476_-475delinsTT
ENST00000371953.7:c.275_276delinsTT	ENSP00000361021.3:p.Asp92Val
ENST00000472832.3:c.275_276delinsTT	ENSP00000483066.2:p.Asp92Val
ENST00000498703.1:n.101_102delinsTT
ENST00000610634.1:c.173_174delinsTT	ENSP00000477517.1:p.Asp58Val
ENST00000686459.1:c.275_276delinsTT	ENSP00000508909.1:p.Asp92Val
ENST00000688158.1:c.*386_*387delinsTT	ENSP00000509254.1:n.*386_*387delinsTT
ENST00000688158.2:n.1010_1011delinsTT
ENST00000688308.1:c.275_276delinsTT	ENSP00000508752.1:p.Asp92Val
ENST00000688922.1:c.196_197delinsTT
ENST00000688922.2:c.*105_*106delinsTT	ENSP00000508742.2:n.*105_*106delinsTT
ENST00000693560.1:c.794_795delinsTT	ENSP00000509861.1:p.Asp265Val
ENST00000700021.1:c.230_231delinsTT	ENSP00000514757.1:p.Asp77Val
ENST00000700022.1:c.275_276delinsTT	ENSP00000514758.1:p.Asp92Val
ENST00000700029.1:c.109_110delinsTT
ENST00000700029.2:c.275_276delinsTT	ENSP00000514759.2:p.Asp92Val
ENST00000706954.1:c.275_276delinsTT	ENSP00000516674.1:p.Asp92Val
ENST00000706955.1:c.*310_*311delinsTT	ENSP00000516675.1:n.*310_*311delinsTT
ENST00000710265.1:c.275_276delinsTT	ENSP00000518161.1:p.Asp92Val
XM_006717926.2:c.230_231delinsTT	XP_006717989.1:p.Asp77Val
XM_011539981.1:c.275_276delinsTT	XP_011538283.1:p.Asp92Val
XM_011539982.1:c.179_180delinsTT	XP_011538284.1:p.Asp60Val
XR_945789.1:n.987_988delinsTT
XR_945790.1:n.987_988delinsTT
XR_945791.1:n.987_988delinsTT