Canonical Allele Identifier: CA891840102

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958009_87958010delinsAA , CM000672.2:g.87958009_87958010delinsAA	GRCh38
NC_000010.10:g.89717766_89717767delinsAA , CM000672.1:g.89717766_89717767delinsAA	GRCh37
NC_000010.9:g.89707746_89707747delinsAA	NCBI36
NG_007466.2:g.99571_99572delinsAA , LRG_311:g.99571_99572delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.791_792delinsAA	ENSP00000514759.2:p.Met264Lys
ENST00000710265.1:c.791_792delinsAA	ENSP00000518161.1:p.Met264Lys
ENST00000472832.3:c.791_792delinsAA	ENSP00000483066.2:p.Met264Lys
ENST00000688158.2:n.1526_1527delinsAA
ENST00000688922.2:c.*621_*622delinsAA	ENSP00000508742.2:n.*621_*622delinsAA
ENST00000700021.1:c.746_747delinsAA	ENSP00000514757.1:p.Met249Lys
ENST00000700022.1:c.*130_*131delinsAA	ENSP00000514758.1:n.*130_*131delinsAA
ENST00000700023.1:n.1949_1950delinsAA
ENST00000700024.1:n.2183_2184delinsAA
ENST00000700025.1:n.1560_1561delinsAA
ENST00000700026.1:n.428_429delinsAA
ENST00000700029.1:c.625_626delinsAA
ENST00000706954.1:c.791_792delinsAA	ENSP00000516674.1:p.Met264Lys
ENST00000706955.1:c.*826_*827delinsAA	ENSP00000516675.1:n.*826_*827delinsAA
ENST00000686459.1:c.*377_*378delinsAA	ENSP00000508909.1:n.*377_*378delinsAA
ENST00000688158.1:c.*902_*903delinsAA	ENSP00000509254.1:n.*902_*903delinsAA
ENST00000688308.1:c.791_792delinsAA	ENSP00000508752.1:p.Met264Lys
ENST00000688922.1:c.712_713delinsAA
ENST00000693560.1:c.1310_1311delinsAA	ENSP00000509861.1:p.Met437Lys
ENST00000371953.8:c.791_792delinsAA MANE Select	ENSP00000361021.3:p.Met264Lys
ENST00000371953.7:c.791_792delinsAA	ENSP00000361021.3:p.Met264Lys
ENST00000472832.2:c.218_219delinsAA	ENSP00000483066.1:p.Met73Lys
NM_000314.5:c.791_792delinsAA	NP_000305.3:p.Met264Lys
NM_000314.6:c.791_792delinsAA	NP_000305.3:p.Met264Lys
NM_001304717.2:c.1310_1311delinsAA	NP_001291646.2:p.Met437Lys
NM_001304718.1:c.200_201delinsAA	NP_001291647.1:p.Met67Lys
XM_006717926.2:c.746_747delinsAA	XP_006717989.1:p.Met249Lys
XM_011539981.1:c.791_792delinsAA	XP_011538283.1:p.Met264Lys
XM_011539982.1:c.695_696delinsAA	XP_011538284.1:p.Met232Lys
XR_945791.1:n.1361_1362delinsAA
NM_000314.7:c.791_792delinsAA	NP_000305.3:p.Met264Lys
NM_001304717.5:c.1310_1311delinsAA	NP_001291646.4:p.Met437Lys
NM_001304718.2:c.200_201delinsAA	NP_001291647.1:p.Met67Lys
NM_000314.8:c.791_792delinsAA MANE Select	NP_000305.3:p.Met264Lys