Canonical Allele Identifier: CA891840619

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957909_87957910delinsAT , CM000672.2:g.87957909_87957910delinsAT	GRCh38
NC_000010.10:g.89717666_89717667delinsAT , CM000672.1:g.89717666_89717667delinsAT	GRCh37
NC_000010.9:g.89707646_89707647delinsAT	NCBI36
NG_007466.2:g.99471_99472delinsAT , LRG_311:g.99471_99472delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.691_692delinsAT	ENSP00000514759.2:p.Pro231Ile
ENST00000710265.1:c.691_692delinsAT	ENSP00000518161.1:p.Pro231Ile
ENST00000472832.3:c.691_692delinsAT	ENSP00000483066.2:p.Pro231Ile
ENST00000688158.2:n.1426_1427delinsAT
ENST00000688922.2:c.*521_*522delinsAT	ENSP00000508742.2:n.*521_*522delinsAT
ENST00000700021.1:c.646_647delinsAT	ENSP00000514757.1:p.Pro216Ile
ENST00000700022.1:c.*30_*31delinsAT	ENSP00000514758.1:n.*30_*31delinsAT
ENST00000700023.1:n.1849_1850delinsAT
ENST00000700024.1:n.2083_2084delinsAT
ENST00000700025.1:n.1460_1461delinsAT
ENST00000700026.1:n.328_329delinsAT
ENST00000700029.1:c.525_526delinsAT
ENST00000706954.1:c.691_692delinsAT	ENSP00000516674.1:p.Pro231Ile
ENST00000706955.1:c.*726_*727delinsAT	ENSP00000516675.1:n.*726_*727delinsAT
ENST00000686459.1:c.*277_*278delinsAT	ENSP00000508909.1:n.*277_*278delinsAT
ENST00000688158.1:c.*802_*803delinsAT	ENSP00000509254.1:n.*802_*803delinsAT
ENST00000688308.1:c.691_692delinsAT	ENSP00000508752.1:p.Pro231Ile
ENST00000688922.1:c.612_613delinsAT
ENST00000693560.1:c.1210_1211delinsAT	ENSP00000509861.1:p.Pro404Ile
ENST00000371953.8:c.691_692delinsAT MANE Select	ENSP00000361021.3:p.Pro231Ile
ENST00000371953.7:c.691_692delinsAT	ENSP00000361021.3:p.Pro231Ile
ENST00000472832.2:c.118_119delinsAT	ENSP00000483066.1:p.Pro40Ile
NM_000314.5:c.691_692delinsAT	NP_000305.3:p.Pro231Ile
NM_000314.6:c.691_692delinsAT	NP_000305.3:p.Pro231Ile
NM_001304717.2:c.1210_1211delinsAT	NP_001291646.2:p.Pro404Ile
NM_001304718.1:c.100_101delinsAT	NP_001291647.1:p.Pro34Ile
XM_006717926.2:c.646_647delinsAT	XP_006717989.1:p.Pro216Ile
XM_011539981.1:c.691_692delinsAT	XP_011538283.1:p.Pro231Ile
XM_011539982.1:c.595_596delinsAT	XP_011538284.1:p.Pro199Ile
XR_945791.1:n.1261_1262delinsAT
NM_000314.7:c.691_692delinsAT	NP_000305.3:p.Pro231Ile
NM_001304717.5:c.1210_1211delinsAT	NP_001291646.4:p.Pro404Ile
NM_001304718.2:c.100_101delinsAT	NP_001291647.1:p.Pro34Ile
NM_000314.8:c.691_692delinsAT MANE Select	NP_000305.3:p.Pro231Ile