Canonical Allele Identifier: CA891840227

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960909_87960911delinsCAA , CM000672.2:g.87960909_87960911delinsCAA	GRCh38
NC_000010.10:g.89720666_89720668delinsCAA , CM000672.1:g.89720666_89720668delinsCAA	GRCh37
NC_000010.9:g.89710646_89710648delinsCAA	NCBI36
NG_007466.2:g.102471_102473delinsCAA , LRG_311:g.102471_102473delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.910_912delinsCAA	ENSP00000514759.2:p.Phe304Gln
ENST00000710265.1:c.817_819delinsCAA	ENSP00000518161.1:p.Phe273Gln
ENST00000472832.3:c.817_819delinsCAA	ENSP00000483066.2:p.Phe273Gln
ENST00000688158.2:n.1552_1554delinsCAA
ENST00000688922.2:c.*647_*649delinsCAA	ENSP00000508742.2:n.*647_*649delinsCAA
ENST00000700021.1:c.772_774delinsCAA	ENSP00000514757.1:p.Phe258Gln
ENST00000700022.1:c.*156_*158delinsCAA	ENSP00000514758.1:n.*156_*158delinsCAA
ENST00000700023.1:n.1975_1977delinsCAA
ENST00000700024.1:n.2209_2211delinsCAA
ENST00000700025.1:n.1586_1588delinsCAA
ENST00000700026.1:n.454_456delinsCAA
ENST00000700029.1:c.744_746delinsCAA
ENST00000706954.1:c.817_819delinsCAA	ENSP00000516674.1:p.Phe273Gln
ENST00000706955.1:c.*852_*854delinsCAA	ENSP00000516675.1:n.*852_*854delinsCAA
ENST00000686459.1:c.*403_*405delinsCAA	ENSP00000508909.1:n.*403_*405delinsCAA
ENST00000688158.1:c.*928_*930delinsCAA	ENSP00000509254.1:n.*928_*930delinsCAA
ENST00000688308.1:c.817_819delinsCAA	ENSP00000508752.1:p.Phe273Gln
ENST00000688922.1:c.738_740delinsCAA
ENST00000693560.1:c.1336_1338delinsCAA	ENSP00000509861.1:p.Phe446Gln
ENST00000371953.8:c.817_819delinsCAA MANE Select	ENSP00000361021.3:p.Phe273Gln
ENST00000371953.7:c.817_819delinsCAA	ENSP00000361021.3:p.Phe273Gln
ENST00000472832.2:c.244_246delinsCAA	ENSP00000483066.1:p.Phe82Gln
NM_000314.5:c.817_819delinsCAA	NP_000305.3:p.Phe273Gln
NM_000314.6:c.817_819delinsCAA	NP_000305.3:p.Phe273Gln
NM_001304717.2:c.1336_1338delinsCAA	NP_001291646.2:p.Phe446Gln
NM_001304718.1:c.226_228delinsCAA	NP_001291647.1:p.Phe76Gln
XM_006717926.2:c.772_774delinsCAA	XP_006717989.1:p.Phe258Gln
XM_011539981.1:c.817_819delinsCAA	XP_011538283.1:p.Phe273Gln
XM_011539982.1:c.721_723delinsCAA	XP_011538284.1:p.Phe241Gln
XR_945791.1:n.1387_1389delinsCAA
NM_000314.7:c.817_819delinsCAA	NP_000305.3:p.Phe273Gln
NM_001304717.5:c.1336_1338delinsCAA	NP_001291646.4:p.Phe446Gln
NM_001304718.2:c.226_228delinsCAA	NP_001291647.1:p.Phe76Gln
NM_000314.8:c.817_819delinsCAA MANE Select	NP_000305.3:p.Phe273Gln