Canonical Allele Identifier: CA1926189956

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960914_87960916delinsGGT , CM000672.2:g.87960914_87960916delinsGGT	GRCh38
NC_000010.10:g.89720671_89720673delinsGGT , CM000672.1:g.89720671_89720673delinsGGT	GRCh37
NC_000010.9:g.89710651_89710653delinsGGT	NCBI36
NG_007466.2:g.102476_102478delinsGGT , LRG_311:g.102476_102478delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.915_917delinsGGT	ENSP00000514759.2:p.Trp305=
ENST00000710265.1:c.822_824delinsGGT	ENSP00000518161.1:p.Trp274=
ENST00000472832.3:c.822_824delinsGGT	ENSP00000483066.2:p.Trp274=
ENST00000688158.2:n.1557_1559delinsGGT
ENST00000688922.2:c.*652_*654delinsGGT	ENSP00000508742.2:n.*652_*654delinsGGT
ENST00000700021.1:c.777_779delinsGGT	ENSP00000514757.1:p.Trp259=
ENST00000700022.1:c.*161_*163delinsGGT	ENSP00000514758.1:n.*161_*163delinsGGT
ENST00000700023.1:n.1980_1982delinsGGT
ENST00000700024.1:n.2214_2216delinsGGT
ENST00000700025.1:n.1591_1593delinsGGT
ENST00000700026.1:n.459_461delinsGGT
ENST00000700029.1:c.749_751delinsGGT
ENST00000706954.1:c.822_824delinsGGT	ENSP00000516674.1:p.Trp274=
ENST00000706955.1:c.*857_*859delinsGGT	ENSP00000516675.1:n.*857_*859delinsGGT
ENST00000686459.1:c.*408_*410delinsGGT	ENSP00000508909.1:n.*408_*410delinsGGT
ENST00000688158.1:c.*933_*935delinsGGT	ENSP00000509254.1:n.*933_*935delinsGGT
ENST00000688308.1:c.822_824delinsGGT	ENSP00000508752.1:p.Trp274=
ENST00000688922.1:c.743_745delinsGGT
ENST00000693560.1:c.1341_1343delinsGGT	ENSP00000509861.1:p.Trp447=
ENST00000371953.8:c.822_824delinsGGT MANE Select	ENSP00000361021.3:p.Trp274=
ENST00000371953.7:c.822_824delinsGGT	ENSP00000361021.3:p.Trp274=
ENST00000472832.2:c.249_251delinsGGT	ENSP00000483066.1:p.Trp83=
NM_000314.5:c.822_824delinsGGT	NP_000305.3:p.Trp274=
NM_000314.6:c.822_824delinsGGT	NP_000305.3:p.Trp274=
NM_001304717.2:c.1341_1343delinsGGT	NP_001291646.2:p.Trp447=
NM_001304718.1:c.231_233delinsGGT	NP_001291647.1:p.Trp77=
XM_006717926.2:c.777_779delinsGGT	XP_006717989.1:p.Trp259=
XM_011539981.1:c.822_824delinsGGT	XP_011538283.1:p.Trp274=
XM_011539982.1:c.726_728delinsGGT	XP_011538284.1:p.Trp242=
XR_945791.1:n.1392_1394delinsGGT
NM_000314.7:c.822_824delinsGGT	NP_000305.3:p.Trp274=
NM_001304717.5:c.1341_1343delinsGGT	NP_001291646.4:p.Trp447=
NM_001304718.2:c.231_233delinsGGT	NP_001291647.1:p.Trp77=
NM_000314.8:c.822_824delinsGGT MANE Select	NP_000305.3:p.Trp274=