Canonical Allele Identifier: CA891836964

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961110_87961112delinsTGG , CM000672.2:g.87961110_87961112delinsTGG	GRCh38
NC_000010.10:g.89720867_89720869delinsTGG , CM000672.1:g.89720867_89720869delinsTGG	GRCh37
NC_000010.9:g.89710847_89710849delinsTGG	NCBI36
NG_007466.2:g.102672_102674delinsTGG , LRG_311:g.102672_102674delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1111_1113delinsTGG	ENSP00000514759.2:p.Asn371Trp
ENST00000710265.1:c.1018_1020delinsTGG	ENSP00000518161.1:p.Asn340Trp
ENST00000472832.3:c.1018_1020delinsTGG	ENSP00000483066.2:p.Asn340Trp
ENST00000688158.2:n.1753_1755delinsTGG
ENST00000688922.2:c.*848_*850delinsTGG	ENSP00000508742.2:n.*848_*850delinsTGG
ENST00000700021.1:c.973_975delinsTGG	ENSP00000514757.1:p.Asn325Trp
ENST00000700022.1:c.*357_*359delinsTGG	ENSP00000514758.1:n.*357_*359delinsTGG
ENST00000700023.1:n.2176_2178delinsTGG
ENST00000700024.1:n.2410_2412delinsTGG
ENST00000700025.1:n.1787_1789delinsTGG
ENST00000700026.1:n.655_657delinsTGG
ENST00000706954.1:c.1018_1020delinsTGG	ENSP00000516674.1:p.Asn340Trp
ENST00000706955.1:c.*1053_*1055delinsTGG	ENSP00000516675.1:n.*1053_*1055delinsTGG
ENST00000686459.1:c.*604_*606delinsTGG	ENSP00000508909.1:n.*604_*606delinsTGG
ENST00000688158.1:c.*1129_*1131delinsTGG	ENSP00000509254.1:n.*1129_*1131delinsTGG
ENST00000688308.1:c.1018_1020delinsTGG	ENSP00000508752.1:p.Asn340Trp
ENST00000688922.1:c.939_941delinsTGG
ENST00000693560.1:c.1537_1539delinsTGG	ENSP00000509861.1:p.Asn513Trp
ENST00000371953.8:c.1018_1020delinsTGG MANE Select	ENSP00000361021.3:p.Asn340Trp
ENST00000371953.7:c.1018_1020delinsTGG	ENSP00000361021.3:p.Asn340Trp
ENST00000472832.2:c.445_447delinsTGG	ENSP00000483066.1:p.Asn149Trp
NM_000314.5:c.1018_1020delinsTGG	NP_000305.3:p.Asn340Trp
NM_000314.6:c.1018_1020delinsTGG	NP_000305.3:p.Asn340Trp
NM_001304717.2:c.1537_1539delinsTGG	NP_001291646.2:p.Asn513Trp
NM_001304718.1:c.427_429delinsTGG	NP_001291647.1:p.Asn143Trp
XM_006717926.2:c.973_975delinsTGG	XP_006717989.1:p.Asn325Trp
XM_011539981.1:c.1018_1020delinsTGG	XP_011538283.1:p.Asn340Trp
XM_011539982.1:c.922_924delinsTGG	XP_011538284.1:p.Asn308Trp
XR_945791.1:n.1588_1590delinsTGG
NM_000314.7:c.1018_1020delinsTGG	NP_000305.3:p.Asn340Trp
NM_001304717.5:c.1537_1539delinsTGG	NP_001291646.4:p.Asn513Trp
NM_001304718.2:c.427_429delinsTGG	NP_001291647.1:p.Asn143Trp
NM_000314.8:c.1018_1020delinsTGG MANE Select	NP_000305.3:p.Asn340Trp