Canonical Allele Identifier: CA891835884

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960999_87961001delinsTGG , CM000672.2:g.87960999_87961001delinsTGG	GRCh38
NC_000010.10:g.89720756_89720758delinsTGG , CM000672.1:g.89720756_89720758delinsTGG	GRCh37
NC_000010.9:g.89710736_89710738delinsTGG	NCBI36
NG_007466.2:g.102561_102563delinsTGG , LRG_311:g.102561_102563delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1000_1002delinsTGG	ENSP00000514759.2:p.Ile334Trp
ENST00000710265.1:c.907_909delinsTGG	ENSP00000518161.1:p.Ile303Trp
ENST00000472832.3:c.907_909delinsTGG	ENSP00000483066.2:p.Ile303Trp
ENST00000688158.2:n.1642_1644delinsTGG
ENST00000688922.2:c.*737_*739delinsTGG	ENSP00000508742.2:n.*737_*739delinsTGG
ENST00000700021.1:c.862_864delinsTGG	ENSP00000514757.1:p.Ile288Trp
ENST00000700022.1:c.*246_*248delinsTGG	ENSP00000514758.1:n.*246_*248delinsTGG
ENST00000700023.1:n.2065_2067delinsTGG
ENST00000700024.1:n.2299_2301delinsTGG
ENST00000700025.1:n.1676_1678delinsTGG
ENST00000700026.1:n.544_546delinsTGG
ENST00000706954.1:c.907_909delinsTGG	ENSP00000516674.1:p.Ile303Trp
ENST00000706955.1:c.*942_*944delinsTGG	ENSP00000516675.1:n.*942_*944delinsTGG
ENST00000686459.1:c.*493_*495delinsTGG	ENSP00000508909.1:n.*493_*495delinsTGG
ENST00000688158.1:c.*1018_*1020delinsTGG	ENSP00000509254.1:n.*1018_*1020delinsTGG
ENST00000688308.1:c.907_909delinsTGG	ENSP00000508752.1:p.Ile303Trp
ENST00000688922.1:c.828_830delinsTGG
ENST00000693560.1:c.1426_1428delinsTGG	ENSP00000509861.1:p.Ile476Trp
ENST00000371953.8:c.907_909delinsTGG MANE Select	ENSP00000361021.3:p.Ile303Trp
ENST00000371953.7:c.907_909delinsTGG	ENSP00000361021.3:p.Ile303Trp
ENST00000472832.2:c.334_336delinsTGG	ENSP00000483066.1:p.Ile112Trp
NM_000314.5:c.907_909delinsTGG	NP_000305.3:p.Ile303Trp
NM_000314.6:c.907_909delinsTGG	NP_000305.3:p.Ile303Trp
NM_001304717.2:c.1426_1428delinsTGG	NP_001291646.2:p.Ile476Trp
NM_001304718.1:c.316_318delinsTGG	NP_001291647.1:p.Ile106Trp
XM_006717926.2:c.862_864delinsTGG	XP_006717989.1:p.Ile288Trp
XM_011539981.1:c.907_909delinsTGG	XP_011538283.1:p.Ile303Trp
XM_011539982.1:c.811_813delinsTGG	XP_011538284.1:p.Ile271Trp
XR_945791.1:n.1477_1479delinsTGG
NM_000314.7:c.907_909delinsTGG	NP_000305.3:p.Ile303Trp
NM_001304717.5:c.1426_1428delinsTGG	NP_001291646.4:p.Ile476Trp
NM_001304718.2:c.316_318delinsTGG	NP_001291647.1:p.Ile106Trp
NM_000314.8:c.907_909delinsTGG MANE Select	NP_000305.3:p.Ile303Trp