Canonical Allele Identifier: CA891834673

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960925_87960926delinsCT , CM000672.2:g.87960925_87960926delinsCT	GRCh38
NC_000010.10:g.89720682_89720683delinsCT , CM000672.1:g.89720682_89720683delinsCT	GRCh37
NC_000010.9:g.89710662_89710663delinsCT	NCBI36
NG_007466.2:g.102487_102488delinsCT , LRG_311:g.102487_102488delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.926_927delinsCT	ENSP00000514759.2:p.Phe309Ser
ENST00000710265.1:c.833_834delinsCT	ENSP00000518161.1:p.Phe278Ser
ENST00000472832.3:c.833_834delinsCT	ENSP00000483066.2:p.Phe278Ser
ENST00000688158.2:n.1568_1569delinsCT
ENST00000688922.2:c.*663_*664delinsCT	ENSP00000508742.2:n.*663_*664delinsCT
ENST00000700021.1:c.788_789delinsCT	ENSP00000514757.1:p.Phe263Ser
ENST00000700022.1:c.*172_*173delinsCT	ENSP00000514758.1:n.*172_*173delinsCT
ENST00000700023.1:n.1991_1992delinsCT
ENST00000700024.1:n.2225_2226delinsCT
ENST00000700025.1:n.1602_1603delinsCT
ENST00000700026.1:n.470_471delinsCT
ENST00000700029.1:c.760_761delinsCT
ENST00000706954.1:c.833_834delinsCT	ENSP00000516674.1:p.Phe278Ser
ENST00000706955.1:c.*868_*869delinsCT	ENSP00000516675.1:n.*868_*869delinsCT
ENST00000686459.1:c.*419_*420delinsCT	ENSP00000508909.1:n.*419_*420delinsCT
ENST00000688158.1:c.*944_*945delinsCT	ENSP00000509254.1:n.*944_*945delinsCT
ENST00000688308.1:c.833_834delinsCT	ENSP00000508752.1:p.Phe278Ser
ENST00000688922.1:c.754_755delinsCT
ENST00000693560.1:c.1352_1353delinsCT	ENSP00000509861.1:p.Phe451Ser
ENST00000371953.8:c.833_834delinsCT MANE Select	ENSP00000361021.3:p.Phe278Ser
ENST00000371953.7:c.833_834delinsCT	ENSP00000361021.3:p.Phe278Ser
ENST00000472832.2:c.260_261delinsCT	ENSP00000483066.1:p.Phe87Ser
NM_000314.5:c.833_834delinsCT	NP_000305.3:p.Phe278Ser
NM_000314.6:c.833_834delinsCT	NP_000305.3:p.Phe278Ser
NM_001304717.2:c.1352_1353delinsCT	NP_001291646.2:p.Phe451Ser
NM_001304718.1:c.242_243delinsCT	NP_001291647.1:p.Phe81Ser
XM_006717926.2:c.788_789delinsCT	XP_006717989.1:p.Phe263Ser
XM_011539981.1:c.833_834delinsCT	XP_011538283.1:p.Phe278Ser
XM_011539982.1:c.737_738delinsCT	XP_011538284.1:p.Phe246Ser
XR_945791.1:n.1403_1404delinsCT
NM_000314.7:c.833_834delinsCT	NP_000305.3:p.Phe278Ser
NM_001304717.5:c.1352_1353delinsCT	NP_001291646.4:p.Phe451Ser
NM_001304718.2:c.242_243delinsCT	NP_001291647.1:p.Phe81Ser
NM_000314.8:c.833_834delinsCT MANE Select	NP_000305.3:p.Phe278Ser