Canonical Allele Identifier: CA891840099

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958009_87958010delinsAT , CM000672.2:g.87958009_87958010delinsAT	GRCh38
NC_000010.10:g.89717766_89717767delinsAT , CM000672.1:g.89717766_89717767delinsAT	GRCh37
NC_000010.9:g.89707746_89707747delinsAT	NCBI36
NG_007466.2:g.99571_99572delinsAT , LRG_311:g.99571_99572delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.791_792delinsAT	ENSP00000514759.2:p.Met264Asn
ENST00000710265.1:c.791_792delinsAT	ENSP00000518161.1:p.Met264Asn
ENST00000472832.3:c.791_792delinsAT	ENSP00000483066.2:p.Met264Asn
ENST00000688158.2:n.1526_1527delinsAT
ENST00000688922.2:c.*621_*622delinsAT	ENSP00000508742.2:n.*621_*622delinsAT
ENST00000700021.1:c.746_747delinsAT	ENSP00000514757.1:p.Met249Asn
ENST00000700022.1:c.*130_*131delinsAT	ENSP00000514758.1:n.*130_*131delinsAT
ENST00000700023.1:n.1949_1950delinsAT
ENST00000700024.1:n.2183_2184delinsAT
ENST00000700025.1:n.1560_1561delinsAT
ENST00000700026.1:n.428_429delinsAT
ENST00000700029.1:c.625_626delinsAT
ENST00000706954.1:c.791_792delinsAT	ENSP00000516674.1:p.Met264Asn
ENST00000706955.1:c.*826_*827delinsAT	ENSP00000516675.1:n.*826_*827delinsAT
ENST00000686459.1:c.*377_*378delinsAT	ENSP00000508909.1:n.*377_*378delinsAT
ENST00000688158.1:c.*902_*903delinsAT	ENSP00000509254.1:n.*902_*903delinsAT
ENST00000688308.1:c.791_792delinsAT	ENSP00000508752.1:p.Met264Asn
ENST00000688922.1:c.712_713delinsAT
ENST00000693560.1:c.1310_1311delinsAT	ENSP00000509861.1:p.Met437Asn
ENST00000371953.8:c.791_792delinsAT MANE Select	ENSP00000361021.3:p.Met264Asn
ENST00000371953.7:c.791_792delinsAT	ENSP00000361021.3:p.Met264Asn
ENST00000472832.2:c.218_219delinsAT	ENSP00000483066.1:p.Met73Asn
NM_000314.5:c.791_792delinsAT	NP_000305.3:p.Met264Asn
NM_000314.6:c.791_792delinsAT	NP_000305.3:p.Met264Asn
NM_001304717.2:c.1310_1311delinsAT	NP_001291646.2:p.Met437Asn
NM_001304718.1:c.200_201delinsAT	NP_001291647.1:p.Met67Asn
XM_006717926.2:c.746_747delinsAT	XP_006717989.1:p.Met249Asn
XM_011539981.1:c.791_792delinsAT	XP_011538283.1:p.Met264Asn
XM_011539982.1:c.695_696delinsAT	XP_011538284.1:p.Met232Asn
XR_945791.1:n.1361_1362delinsAT
NM_000314.7:c.791_792delinsAT	NP_000305.3:p.Met264Asn
NM_001304717.5:c.1310_1311delinsAT	NP_001291646.4:p.Met437Asn
NM_001304718.2:c.200_201delinsAT	NP_001291647.1:p.Met67Asn
NM_000314.8:c.791_792delinsAT MANE Select	NP_000305.3:p.Met264Asn