Canonical Allele Identifier: CA891841734

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965467_87965469delinsGTC , CM000672.2:g.87965467_87965469delinsGTC	GRCh38
NC_000010.10:g.89725224_89725226delinsGTC , CM000672.1:g.89725224_89725226delinsGTC	GRCh37
NC_000010.9:g.89715204_89715206delinsGTC	NCBI36
NG_007466.2:g.107029_107031delinsGTC , LRG_311:g.107029_107031delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1300_1302delinsGTC	ENSP00000514759.2:p.Val434=
ENST00000710265.1:c.*236_*238delinsGTC	ENSP00000518161.1:n.*236_*238delinsGTC
ENST00000688158.2:n.1942_1944delinsGTC
ENST00000688922.2:c.*1037_*1039delinsGTC	ENSP00000508742.2:n.*1037_*1039delinsGTC
ENST00000700021.1:c.1162_1164delinsGTC	ENSP00000514757.1:p.Val388=
ENST00000700022.1:c.*546_*548delinsGTC	ENSP00000514758.1:n.*546_*548delinsGTC
ENST00000700023.1:n.2365_2367delinsGTC
ENST00000700024.1:n.2599_2601delinsGTC
ENST00000706954.1:c.1207_1209delinsGTC	ENSP00000516674.1:p.Val403=
ENST00000706955.1:c.*1242_*1244delinsGTC	ENSP00000516675.1:n.*1242_*1244delinsGTC
ENST00000686459.1:c.*793_*795delinsGTC	ENSP00000508909.1:n.*793_*795delinsGTC
ENST00000688158.1:c.*1318_*1320delinsGTC	ENSP00000509254.1:n.*1318_*1320delinsGTC
ENST00000688308.1:c.1207_1209delinsGTC	ENSP00000508752.1:p.Val403=
ENST00000688922.1:c.1128_1130delinsGTC
ENST00000693560.1:c.1726_1728delinsGTC	ENSP00000509861.1:p.Val576=
ENST00000371953.8:c.1207_1209delinsGTC MANE Select	ENSP00000361021.3:p.Val403=
ENST00000371953.7:c.1207_1209delinsGTC	ENSP00000361021.3:p.Val403=
NM_000314.5:c.1207_1209delinsGTC	NP_000305.3:p.Val403=
NM_000314.6:c.1207_1209delinsGTC	NP_000305.3:p.Val403=
NM_001304717.2:c.1726_1728delinsGTC	NP_001291646.2:p.Val576=
NM_001304718.1:c.616_618delinsGTC	NP_001291647.1:p.Val206=
XM_006717926.2:c.1162_1164delinsGTC	XP_006717989.1:p.Val388=
XM_011539982.1:c.1111_1113delinsGTC	XP_011538284.1:p.Val371=
XR_945791.1:n.1777_1779delinsGTC
NM_000314.7:c.1207_1209delinsGTC	NP_000305.3:p.Val403=
NM_001304717.5:c.1726_1728delinsGTC	NP_001291646.4:p.Val576=
NM_001304718.2:c.616_618delinsGTC	NP_001291647.1:p.Val206=
NM_000314.8:c.1207_1209delinsGTC MANE Select	NP_000305.3:p.Val403=