Canonical Allele Identifier: CA891838166

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965446_87965448delinsGTT , CM000672.2:g.87965446_87965448delinsGTT	GRCh38
NC_000010.10:g.89725203_89725205delinsGTT , CM000672.1:g.89725203_89725205delinsGTT	GRCh37
NC_000010.9:g.89715183_89715185delinsGTT	NCBI36
NG_007466.2:g.107008_107010delinsGTT , LRG_311:g.107008_107010delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1279_1281delinsGTT	ENSP00000514759.2:p.Gln427Val
ENST00000710265.1:c.*215_*217delinsGTT	ENSP00000518161.1:n.*215_*217delinsGTT
ENST00000688158.2:n.1921_1923delinsGTT
ENST00000688922.2:c.*1016_*1018delinsGTT	ENSP00000508742.2:n.*1016_*1018delinsGTT
ENST00000700021.1:c.1141_1143delinsGTT	ENSP00000514757.1:p.Gln381Val
ENST00000700022.1:c.*525_*527delinsGTT	ENSP00000514758.1:n.*525_*527delinsGTT
ENST00000700023.1:n.2344_2346delinsGTT
ENST00000700024.1:n.2578_2580delinsGTT
ENST00000706954.1:c.1186_1188delinsGTT	ENSP00000516674.1:p.Gln396Val
ENST00000706955.1:c.*1221_*1223delinsGTT	ENSP00000516675.1:n.*1221_*1223delinsGTT
ENST00000686459.1:c.*772_*774delinsGTT	ENSP00000508909.1:n.*772_*774delinsGTT
ENST00000688158.1:c.*1297_*1299delinsGTT	ENSP00000509254.1:n.*1297_*1299delinsGTT
ENST00000688308.1:c.1186_1188delinsGTT	ENSP00000508752.1:p.Gln396Val
ENST00000688922.1:c.1107_1109delinsGTT
ENST00000693560.1:c.1705_1707delinsGTT	ENSP00000509861.1:p.Gln569Val
ENST00000371953.8:c.1186_1188delinsGTT MANE Select	ENSP00000361021.3:p.Gln396Val
ENST00000371953.7:c.1186_1188delinsGTT	ENSP00000361021.3:p.Gln396Val
NM_000314.5:c.1186_1188delinsGTT	NP_000305.3:p.Gln396Val
NM_000314.6:c.1186_1188delinsGTT	NP_000305.3:p.Gln396Val
NM_001304717.2:c.1705_1707delinsGTT	NP_001291646.2:p.Gln569Val
NM_001304718.1:c.595_597delinsGTT	NP_001291647.1:p.Gln199Val
XM_006717926.2:c.1141_1143delinsGTT	XP_006717989.1:p.Gln381Val
XM_011539982.1:c.1090_1092delinsGTT	XP_011538284.1:p.Gln364Val
XR_945791.1:n.1756_1758delinsGTT
NM_000314.7:c.1186_1188delinsGTT	NP_000305.3:p.Gln396Val
NM_001304717.5:c.1705_1707delinsGTT	NP_001291646.4:p.Gln569Val
NM_001304718.2:c.595_597delinsGTT	NP_001291647.1:p.Gln199Val
NM_000314.8:c.1186_1188delinsGTT MANE Select	NP_000305.3:p.Gln396Val