Canonical Allele Identifier: CA891840247

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960913_87960914delinsCT , CM000672.2:g.87960913_87960914delinsCT	GRCh38
NC_000010.10:g.89720670_89720671delinsCT , CM000672.1:g.89720670_89720671delinsCT	GRCh37
NC_000010.9:g.89710650_89710651delinsCT	NCBI36
NG_007466.2:g.102475_102476delinsCT , LRG_311:g.102475_102476delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.914_915delinsCT	ENSP00000514759.2:p.Trp305Ser
ENST00000710265.1:c.821_822delinsCT	ENSP00000518161.1:p.Trp274Ser
ENST00000472832.3:c.821_822delinsCT	ENSP00000483066.2:p.Trp274Ser
ENST00000688158.2:n.1556_1557delinsCT
ENST00000688922.2:c.*651_*652delinsCT	ENSP00000508742.2:n.*651_*652delinsCT
ENST00000700021.1:c.776_777delinsCT	ENSP00000514757.1:p.Trp259Ser
ENST00000700022.1:c.*160_*161delinsCT	ENSP00000514758.1:n.*160_*161delinsCT
ENST00000700023.1:n.1979_1980delinsCT
ENST00000700024.1:n.2213_2214delinsCT
ENST00000700025.1:n.1590_1591delinsCT
ENST00000700026.1:n.458_459delinsCT
ENST00000700029.1:c.748_749delinsCT
ENST00000706954.1:c.821_822delinsCT	ENSP00000516674.1:p.Trp274Ser
ENST00000706955.1:c.*856_*857delinsCT	ENSP00000516675.1:n.*856_*857delinsCT
ENST00000686459.1:c.*407_*408delinsCT	ENSP00000508909.1:n.*407_*408delinsCT
ENST00000688158.1:c.*932_*933delinsCT	ENSP00000509254.1:n.*932_*933delinsCT
ENST00000688308.1:c.821_822delinsCT	ENSP00000508752.1:p.Trp274Ser
ENST00000688922.1:c.742_743delinsCT
ENST00000693560.1:c.1340_1341delinsCT	ENSP00000509861.1:p.Trp447Ser
ENST00000371953.8:c.821_822delinsCT MANE Select	ENSP00000361021.3:p.Trp274Ser
ENST00000371953.7:c.821_822delinsCT	ENSP00000361021.3:p.Trp274Ser
ENST00000472832.2:c.248_249delinsCT	ENSP00000483066.1:p.Trp83Ser
NM_000314.5:c.821_822delinsCT	NP_000305.3:p.Trp274Ser
NM_000314.6:c.821_822delinsCT	NP_000305.3:p.Trp274Ser
NM_001304717.2:c.1340_1341delinsCT	NP_001291646.2:p.Trp447Ser
NM_001304718.1:c.230_231delinsCT	NP_001291647.1:p.Trp77Ser
XM_006717926.2:c.776_777delinsCT	XP_006717989.1:p.Trp259Ser
XM_011539981.1:c.821_822delinsCT	XP_011538283.1:p.Trp274Ser
XM_011539982.1:c.725_726delinsCT	XP_011538284.1:p.Trp242Ser
XR_945791.1:n.1391_1392delinsCT
NM_000314.7:c.821_822delinsCT	NP_000305.3:p.Trp274Ser
NM_001304717.5:c.1340_1341delinsCT	NP_001291646.4:p.Trp447Ser
NM_001304718.2:c.230_231delinsCT	NP_001291647.1:p.Trp77Ser
NM_000314.8:c.821_822delinsCT MANE Select	NP_000305.3:p.Trp274Ser