Canonical Allele Identifier: CA891840225

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960909_87960911delinsAGA , CM000672.2:g.87960909_87960911delinsAGA	GRCh38
NC_000010.10:g.89720666_89720668delinsAGA , CM000672.1:g.89720666_89720668delinsAGA	GRCh37
NC_000010.9:g.89710646_89710648delinsAGA	NCBI36
NG_007466.2:g.102471_102473delinsAGA , LRG_311:g.102471_102473delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.910_912delinsAGA	ENSP00000514759.2:p.Phe304Arg
ENST00000710265.1:c.817_819delinsAGA	ENSP00000518161.1:p.Phe273Arg
ENST00000472832.3:c.817_819delinsAGA	ENSP00000483066.2:p.Phe273Arg
ENST00000688158.2:n.1552_1554delinsAGA
ENST00000688922.2:c.*647_*649delinsAGA	ENSP00000508742.2:n.*647_*649delinsAGA
ENST00000700021.1:c.772_774delinsAGA	ENSP00000514757.1:p.Phe258Arg
ENST00000700022.1:c.*156_*158delinsAGA	ENSP00000514758.1:n.*156_*158delinsAGA
ENST00000700023.1:n.1975_1977delinsAGA
ENST00000700024.1:n.2209_2211delinsAGA
ENST00000700025.1:n.1586_1588delinsAGA
ENST00000700026.1:n.454_456delinsAGA
ENST00000700029.1:c.744_746delinsAGA
ENST00000706954.1:c.817_819delinsAGA	ENSP00000516674.1:p.Phe273Arg
ENST00000706955.1:c.*852_*854delinsAGA	ENSP00000516675.1:n.*852_*854delinsAGA
ENST00000686459.1:c.*403_*405delinsAGA	ENSP00000508909.1:n.*403_*405delinsAGA
ENST00000688158.1:c.*928_*930delinsAGA	ENSP00000509254.1:n.*928_*930delinsAGA
ENST00000688308.1:c.817_819delinsAGA	ENSP00000508752.1:p.Phe273Arg
ENST00000688922.1:c.738_740delinsAGA
ENST00000693560.1:c.1336_1338delinsAGA	ENSP00000509861.1:p.Phe446Arg
ENST00000371953.8:c.817_819delinsAGA MANE Select	ENSP00000361021.3:p.Phe273Arg
ENST00000371953.7:c.817_819delinsAGA	ENSP00000361021.3:p.Phe273Arg
ENST00000472832.2:c.244_246delinsAGA	ENSP00000483066.1:p.Phe82Arg
NM_000314.5:c.817_819delinsAGA	NP_000305.3:p.Phe273Arg
NM_000314.6:c.817_819delinsAGA	NP_000305.3:p.Phe273Arg
NM_001304717.2:c.1336_1338delinsAGA	NP_001291646.2:p.Phe446Arg
NM_001304718.1:c.226_228delinsAGA	NP_001291647.1:p.Phe76Arg
XM_006717926.2:c.772_774delinsAGA	XP_006717989.1:p.Phe258Arg
XM_011539981.1:c.817_819delinsAGA	XP_011538283.1:p.Phe273Arg
XM_011539982.1:c.721_723delinsAGA	XP_011538284.1:p.Phe241Arg
XR_945791.1:n.1387_1389delinsAGA
NM_000314.7:c.817_819delinsAGA	NP_000305.3:p.Phe273Arg
NM_001304717.5:c.1336_1338delinsAGA	NP_001291646.4:p.Phe446Arg
NM_001304718.2:c.226_228delinsAGA	NP_001291647.1:p.Phe76Arg
NM_000314.8:c.817_819delinsAGA MANE Select	NP_000305.3:p.Phe273Arg