Canonical Allele Identifier: CA891839296

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952256_87952258delinsGTT , CM000672.2:g.87952256_87952258delinsGTT	GRCh38
NC_000010.10:g.89712013_89712015delinsGTT , CM000672.1:g.89712013_89712015delinsGTT	GRCh37
NC_000010.9:g.89701993_89701995delinsGTT	NCBI36
NG_007466.2:g.93818_93820delinsGTT , LRG_311:g.93818_93820delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.631_633delinsGTT	ENSP00000514759.2:p.Cys211Val
ENST00000710265.1:c.631_633delinsGTT	ENSP00000518161.1:p.Cys211Val
ENST00000472832.3:c.631_633delinsGTT	ENSP00000483066.2:p.Cys211Val
ENST00000688158.2:n.1366_1368delinsGTT
ENST00000688922.2:c.*461_*463delinsGTT	ENSP00000508742.2:n.*461_*463delinsGTT
ENST00000700021.1:c.586_588delinsGTT	ENSP00000514757.1:p.Cys196Val
ENST00000700022.1:c.493-5597_493-5595delinsGTT	ENSP00000514758.1:n.493-5597_493-5595delinsGTT
ENST00000700023.1:n.1789_1791delinsGTT
ENST00000700024.1:n.2023_2025delinsGTT
ENST00000700025.1:n.1400_1402delinsGTT
ENST00000700029.1:c.465_467delinsGTT
ENST00000706954.1:c.631_633delinsGTT	ENSP00000516674.1:p.Cys211Val
ENST00000706955.1:c.*666_*668delinsGTT	ENSP00000516675.1:n.*666_*668delinsGTT
ENST00000686459.1:c.*217_*219delinsGTT	ENSP00000508909.1:n.*217_*219delinsGTT
ENST00000688158.1:c.*742_*744delinsGTT	ENSP00000509254.1:n.*742_*744delinsGTT
ENST00000688308.1:c.631_633delinsGTT	ENSP00000508752.1:p.Cys211Val
ENST00000688922.1:c.552_554delinsGTT
ENST00000693560.1:c.1150_1152delinsGTT	ENSP00000509861.1:p.Cys384Val
ENST00000371953.8:c.631_633delinsGTT MANE Select	ENSP00000361021.3:p.Cys211Val
ENST00000371953.7:c.631_633delinsGTT	ENSP00000361021.3:p.Cys211Val
ENST00000472832.2:c.58_60delinsGTT	ENSP00000483066.1:p.Cys20Val
NM_000314.5:c.631_633delinsGTT	NP_000305.3:p.Cys211Val
NM_000314.6:c.631_633delinsGTT	NP_000305.3:p.Cys211Val
NM_001304717.2:c.1150_1152delinsGTT	NP_001291646.2:p.Cys384Val
NM_001304718.1:c.40_42delinsGTT	NP_001291647.1:p.Cys14Val
XM_006717926.2:c.586_588delinsGTT	XP_006717989.1:p.Cys196Val
XM_011539981.1:c.631_633delinsGTT	XP_011538283.1:p.Cys211Val
XM_011539982.1:c.535_537delinsGTT	XP_011538284.1:p.Cys179Val
XR_945791.1:n.1205-5597_1205-5595delinsGTT
NM_000314.7:c.631_633delinsGTT	NP_000305.3:p.Cys211Val
NM_001304717.5:c.1150_1152delinsGTT	NP_001291646.4:p.Cys384Val
NM_001304718.2:c.40_42delinsGTT	NP_001291647.1:p.Cys14Val
NM_000314.8:c.631_633delinsGTT MANE Select	NP_000305.3:p.Cys211Val