Canonical Allele Identifier: CA2579926732

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960934_87960935delinsAT , CM000672.2:g.87960934_87960935delinsAT	GRCh38
NC_000010.10:g.89720691_89720692delinsAT , CM000672.1:g.89720691_89720692delinsAT	GRCh37
NC_000010.9:g.89710671_89710672delinsAT	NCBI36
NG_007466.2:g.102496_102497delinsAT , LRG_311:g.102496_102497delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.935_936delinsAT	ENSP00000514759.2:p.Pro312His
ENST00000710265.1:c.842_843delinsAT	ENSP00000518161.1:p.Pro281His
ENST00000472832.3:c.842_843delinsAT	ENSP00000483066.2:p.Pro281His
ENST00000688158.2:n.1577_1578delinsAT
ENST00000688922.2:c.*672_*673delinsAT	ENSP00000508742.2:n.*672_*673delinsAT
ENST00000700021.1:c.797_798delinsAT	ENSP00000514757.1:p.Pro266His
ENST00000700022.1:c.*181_*182delinsAT	ENSP00000514758.1:n.*181_*182delinsAT
ENST00000700023.1:n.2000_2001delinsAT
ENST00000700024.1:n.2234_2235delinsAT
ENST00000700025.1:n.1611_1612delinsAT
ENST00000700026.1:n.479_480delinsAT
ENST00000700029.1:c.769_770delinsAT
ENST00000706954.1:c.842_843delinsAT	ENSP00000516674.1:p.Pro281His
ENST00000706955.1:c.*877_*878delinsAT	ENSP00000516675.1:n.*877_*878delinsAT
ENST00000686459.1:c.*428_*429delinsAT	ENSP00000508909.1:n.*428_*429delinsAT
ENST00000688158.1:c.*953_*954delinsAT	ENSP00000509254.1:n.*953_*954delinsAT
ENST00000688308.1:c.842_843delinsAT	ENSP00000508752.1:p.Pro281His
ENST00000688922.1:c.763_764delinsAT
ENST00000693560.1:c.1361_1362delinsAT	ENSP00000509861.1:p.Pro454His
ENST00000371953.8:c.842_843delinsAT MANE Select	ENSP00000361021.3:p.Pro281His
ENST00000371953.7:c.842_843delinsAT	ENSP00000361021.3:p.Pro281His
ENST00000472832.2:c.269_270delinsAT	ENSP00000483066.1:p.Pro90His
NM_000314.5:c.842_843delinsAT	NP_000305.3:p.Pro281His
NM_000314.6:c.842_843delinsAT	NP_000305.3:p.Pro281His
NM_001304717.2:c.1361_1362delinsAT	NP_001291646.2:p.Pro454His
NM_001304718.1:c.251_252delinsAT	NP_001291647.1:p.Pro84His
XM_006717926.2:c.797_798delinsAT	XP_006717989.1:p.Pro266His
XM_011539981.1:c.842_843delinsAT	XP_011538283.1:p.Pro281His
XM_011539982.1:c.746_747delinsAT	XP_011538284.1:p.Pro249His
XR_945791.1:n.1412_1413delinsAT
NM_000314.7:c.842_843delinsAT	NP_000305.3:p.Pro281His
NM_001304717.5:c.1361_1362delinsAT	NP_001291646.4:p.Pro454His
NM_001304718.2:c.251_252delinsAT	NP_001291647.1:p.Pro84His
NM_000314.8:c.842_843delinsAT MANE Select	NP_000305.3:p.Pro281His