Canonical Allele Identifier: CA891840176

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960898_87960899delinsTG , CM000672.2:g.87960898_87960899delinsTG	GRCh38
NC_000010.10:g.89720655_89720656delinsTG , CM000672.1:g.89720655_89720656delinsTG	GRCh37
NC_000010.9:g.89710635_89710636delinsTG	NCBI36
NG_007466.2:g.102460_102461delinsTG , LRG_311:g.102460_102461delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.899_900delinsTG	ENSP00000514759.2:p.Lys300Met
ENST00000710265.1:c.806_807delinsTG	ENSP00000518161.1:p.Lys269Met
ENST00000472832.3:c.806_807delinsTG	ENSP00000483066.2:p.Lys269Met
ENST00000688158.2:n.1541_1542delinsTG
ENST00000688922.2:c.*636_*637delinsTG	ENSP00000508742.2:n.*636_*637delinsTG
ENST00000700021.1:c.761_762delinsTG	ENSP00000514757.1:p.Lys254Met
ENST00000700022.1:c.*145_*146delinsTG	ENSP00000514758.1:n.*145_*146delinsTG
ENST00000700023.1:n.1964_1965delinsTG
ENST00000700024.1:n.2198_2199delinsTG
ENST00000700025.1:n.1575_1576delinsTG
ENST00000700026.1:n.443_444delinsTG
ENST00000700029.1:c.733_734delinsTG
ENST00000706954.1:c.806_807delinsTG	ENSP00000516674.1:p.Lys269Met
ENST00000706955.1:c.*841_*842delinsTG	ENSP00000516675.1:n.*841_*842delinsTG
ENST00000686459.1:c.*392_*393delinsTG	ENSP00000508909.1:n.*392_*393delinsTG
ENST00000688158.1:c.*917_*918delinsTG	ENSP00000509254.1:n.*917_*918delinsTG
ENST00000688308.1:c.806_807delinsTG	ENSP00000508752.1:p.Lys269Met
ENST00000688922.1:c.727_728delinsTG
ENST00000693560.1:c.1325_1326delinsTG	ENSP00000509861.1:p.Lys442Met
ENST00000371953.8:c.806_807delinsTG MANE Select	ENSP00000361021.3:p.Lys269Met
ENST00000371953.7:c.806_807delinsTG	ENSP00000361021.3:p.Lys269Met
ENST00000472832.2:c.233_234delinsTG	ENSP00000483066.1:p.Lys78Met
NM_000314.5:c.806_807delinsTG	NP_000305.3:p.Lys269Met
NM_000314.6:c.806_807delinsTG	NP_000305.3:p.Lys269Met
NM_001304717.2:c.1325_1326delinsTG	NP_001291646.2:p.Lys442Met
NM_001304718.1:c.215_216delinsTG	NP_001291647.1:p.Lys72Met
XM_006717926.2:c.761_762delinsTG	XP_006717989.1:p.Lys254Met
XM_011539981.1:c.806_807delinsTG	XP_011538283.1:p.Lys269Met
XM_011539982.1:c.710_711delinsTG	XP_011538284.1:p.Lys237Met
XR_945791.1:n.1376_1377delinsTG
NM_000314.7:c.806_807delinsTG	NP_000305.3:p.Lys269Met
NM_001304717.5:c.1325_1326delinsTG	NP_001291646.4:p.Lys442Met
NM_001304718.2:c.215_216delinsTG	NP_001291647.1:p.Lys72Met
NM_000314.8:c.806_807delinsTG MANE Select	NP_000305.3:p.Lys269Met