Canonical Allele Identifier: CA891840165

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960897_87960899delinsTGT , CM000672.2:g.87960897_87960899delinsTGT	GRCh38
NC_000010.10:g.89720654_89720656delinsTGT , CM000672.1:g.89720654_89720656delinsTGT	GRCh37
NC_000010.9:g.89710634_89710636delinsTGT	NCBI36
NG_007466.2:g.102459_102461delinsTGT , LRG_311:g.102459_102461delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.898_900delinsTGT	ENSP00000514759.2:p.Lys300Cys
ENST00000710265.1:c.805_807delinsTGT	ENSP00000518161.1:p.Lys269Cys
ENST00000472832.3:c.805_807delinsTGT	ENSP00000483066.2:p.Lys269Cys
ENST00000688158.2:n.1540_1542delinsTGT
ENST00000688922.2:c.*635_*637delinsTGT	ENSP00000508742.2:n.*635_*637delinsTGT
ENST00000700021.1:c.760_762delinsTGT	ENSP00000514757.1:p.Lys254Cys
ENST00000700022.1:c.*144_*146delinsTGT	ENSP00000514758.1:n.*144_*146delinsTGT
ENST00000700023.1:n.1963_1965delinsTGT
ENST00000700024.1:n.2197_2199delinsTGT
ENST00000700025.1:n.1574_1576delinsTGT
ENST00000700026.1:n.442_444delinsTGT
ENST00000700029.1:c.732_734delinsTGT
ENST00000706954.1:c.805_807delinsTGT	ENSP00000516674.1:p.Lys269Cys
ENST00000706955.1:c.*840_*842delinsTGT	ENSP00000516675.1:n.*840_*842delinsTGT
ENST00000686459.1:c.*391_*393delinsTGT	ENSP00000508909.1:n.*391_*393delinsTGT
ENST00000688158.1:c.*916_*918delinsTGT	ENSP00000509254.1:n.*916_*918delinsTGT
ENST00000688308.1:c.805_807delinsTGT	ENSP00000508752.1:p.Lys269Cys
ENST00000688922.1:c.726_728delinsTGT
ENST00000693560.1:c.1324_1326delinsTGT	ENSP00000509861.1:p.Lys442Cys
ENST00000371953.8:c.805_807delinsTGT MANE Select	ENSP00000361021.3:p.Lys269Cys
ENST00000371953.7:c.805_807delinsTGT	ENSP00000361021.3:p.Lys269Cys
ENST00000472832.2:c.232_234delinsTGT	ENSP00000483066.1:p.Lys78Cys
NM_000314.5:c.805_807delinsTGT	NP_000305.3:p.Lys269Cys
NM_000314.6:c.805_807delinsTGT	NP_000305.3:p.Lys269Cys
NM_001304717.2:c.1324_1326delinsTGT	NP_001291646.2:p.Lys442Cys
NM_001304718.1:c.214_216delinsTGT	NP_001291647.1:p.Lys72Cys
XM_006717926.2:c.760_762delinsTGT	XP_006717989.1:p.Lys254Cys
XM_011539981.1:c.805_807delinsTGT	XP_011538283.1:p.Lys269Cys
XM_011539982.1:c.709_711delinsTGT	XP_011538284.1:p.Lys237Cys
XR_945791.1:n.1375_1377delinsTGT
NM_000314.7:c.805_807delinsTGT	NP_000305.3:p.Lys269Cys
NM_001304717.5:c.1324_1326delinsTGT	NP_001291646.4:p.Lys442Cys
NM_001304718.2:c.214_216delinsTGT	NP_001291647.1:p.Lys72Cys
NM_000314.8:c.805_807delinsTGT MANE Select	NP_000305.3:p.Lys269Cys