Canonical Allele Identifier: CA891840101

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958009_87958010delinsGA , CM000672.2:g.87958009_87958010delinsGA	GRCh38
NC_000010.10:g.89717766_89717767delinsGA , CM000672.1:g.89717766_89717767delinsGA	GRCh37
NC_000010.9:g.89707746_89707747delinsGA	NCBI36
NG_007466.2:g.99571_99572delinsGA , LRG_311:g.99571_99572delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.791_792delinsGA	ENSP00000514759.2:p.Met264Arg
ENST00000710265.1:c.791_792delinsGA	ENSP00000518161.1:p.Met264Arg
ENST00000472832.3:c.791_792delinsGA	ENSP00000483066.2:p.Met264Arg
ENST00000688158.2:n.1526_1527delinsGA
ENST00000688922.2:c.*621_*622delinsGA	ENSP00000508742.2:n.*621_*622delinsGA
ENST00000700021.1:c.746_747delinsGA	ENSP00000514757.1:p.Met249Arg
ENST00000700022.1:c.*130_*131delinsGA	ENSP00000514758.1:n.*130_*131delinsGA
ENST00000700023.1:n.1949_1950delinsGA
ENST00000700024.1:n.2183_2184delinsGA
ENST00000700025.1:n.1560_1561delinsGA
ENST00000700026.1:n.428_429delinsGA
ENST00000700029.1:c.625_626delinsGA
ENST00000706954.1:c.791_792delinsGA	ENSP00000516674.1:p.Met264Arg
ENST00000706955.1:c.*826_*827delinsGA	ENSP00000516675.1:n.*826_*827delinsGA
ENST00000686459.1:c.*377_*378delinsGA	ENSP00000508909.1:n.*377_*378delinsGA
ENST00000688158.1:c.*902_*903delinsGA	ENSP00000509254.1:n.*902_*903delinsGA
ENST00000688308.1:c.791_792delinsGA	ENSP00000508752.1:p.Met264Arg
ENST00000688922.1:c.712_713delinsGA
ENST00000693560.1:c.1310_1311delinsGA	ENSP00000509861.1:p.Met437Arg
ENST00000371953.8:c.791_792delinsGA MANE Select	ENSP00000361021.3:p.Met264Arg
ENST00000371953.7:c.791_792delinsGA	ENSP00000361021.3:p.Met264Arg
ENST00000472832.2:c.218_219delinsGA	ENSP00000483066.1:p.Met73Arg
NM_000314.5:c.791_792delinsGA	NP_000305.3:p.Met264Arg
NM_000314.6:c.791_792delinsGA	NP_000305.3:p.Met264Arg
NM_001304717.2:c.1310_1311delinsGA	NP_001291646.2:p.Met437Arg
NM_001304718.1:c.200_201delinsGA	NP_001291647.1:p.Met67Arg
XM_006717926.2:c.746_747delinsGA	XP_006717989.1:p.Met249Arg
XM_011539981.1:c.791_792delinsGA	XP_011538283.1:p.Met264Arg
XM_011539982.1:c.695_696delinsGA	XP_011538284.1:p.Met232Arg
XR_945791.1:n.1361_1362delinsGA
NM_000314.7:c.791_792delinsGA	NP_000305.3:p.Met264Arg
NM_001304717.5:c.1310_1311delinsGA	NP_001291646.4:p.Met437Arg
NM_001304718.2:c.200_201delinsGA	NP_001291647.1:p.Met67Arg
NM_000314.8:c.791_792delinsGA MANE Select	NP_000305.3:p.Met264Arg