Canonical Allele Identifier: CA891840078
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958005_87958006delinsTG , CM000672.2:g.87958005_87958006delinsTG GRCh38
NC_000010.10:g.89717762_89717763delinsTG , CM000672.1:g.89717762_89717763delinsTG GRCh37
NC_000010.9:g.89707742_89707743delinsTG NCBI36
NG_007466.2:g.99567_99568delinsTG , LRG_311:g.99567_99568delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.787_788delinsTG ENSP00000514759.2:p.Lys263Trp
ENST00000710265.1:c.787_788delinsTG ENSP00000518161.1:p.Lys263Trp
ENST00000472832.3:c.787_788delinsTG ENSP00000483066.2:p.Lys263Trp
ENST00000688158.2:n.1522_1523delinsTG
ENST00000688922.2:c.*617_*618delinsTG ENSP00000508742.2:n.*617_*618delinsTG
ENST00000700021.1:c.742_743delinsTG ENSP00000514757.1:p.Lys248Trp
ENST00000700022.1:c.*126_*127delinsTG ENSP00000514758.1:n.*126_*127delinsTG
ENST00000700023.1:n.1945_1946delinsTG
ENST00000700024.1:n.2179_2180delinsTG
ENST00000700025.1:n.1556_1557delinsTG
ENST00000700026.1:n.424_425delinsTG
ENST00000700029.1:c.621_622delinsTG
ENST00000706954.1:c.787_788delinsTG ENSP00000516674.1:p.Lys263Trp
ENST00000706955.1:c.*822_*823delinsTG ENSP00000516675.1:n.*822_*823delinsTG
ENST00000686459.1:c.*373_*374delinsTG ENSP00000508909.1:n.*373_*374delinsTG
ENST00000688158.1:c.*898_*899delinsTG ENSP00000509254.1:n.*898_*899delinsTG
ENST00000688308.1:c.787_788delinsTG ENSP00000508752.1:p.Lys263Trp
ENST00000688922.1:c.708_709delinsTG
ENST00000693560.1:c.1306_1307delinsTG ENSP00000509861.1:p.Lys436Trp
ENST00000371953.8:c.787_788delinsTG MANE Select ENSP00000361021.3:p.Lys263Trp
ENST00000371953.7:c.787_788delinsTG ENSP00000361021.3:p.Lys263Trp
ENST00000472832.2:c.214_215delinsTG ENSP00000483066.1:p.Lys72Trp
NM_000314.5:c.787_788delinsTG NP_000305.3:p.Lys263Trp
NM_000314.6:c.787_788delinsTG NP_000305.3:p.Lys263Trp
NM_001304717.2:c.1306_1307delinsTG NP_001291646.2:p.Lys436Trp
NM_001304718.1:c.196_197delinsTG NP_001291647.1:p.Lys66Trp
XM_006717926.2:c.742_743delinsTG XP_006717989.1:p.Lys248Trp
XM_011539981.1:c.787_788delinsTG XP_011538283.1:p.Lys263Trp
XM_011539982.1:c.691_692delinsTG XP_011538284.1:p.Lys231Trp
XR_945791.1:n.1357_1358delinsTG
NM_000314.7:c.787_788delinsTG NP_000305.3:p.Lys263Trp
NM_001304717.5:c.1306_1307delinsTG NP_001291646.4:p.Lys436Trp
NM_001304718.2:c.196_197delinsTG NP_001291647.1:p.Lys66Trp
NM_000314.8:c.787_788delinsTG MANE Select NP_000305.3:p.Lys263Trp