Canonical Allele Identifier: CA891840948
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958005_87958006delinsTC , CM000672.2:g.87958005_87958006delinsTC GRCh38
NC_000010.10:g.89717762_89717763delinsTC , CM000672.1:g.89717762_89717763delinsTC GRCh37
NC_000010.9:g.89707742_89707743delinsTC NCBI36
NG_007466.2:g.99567_99568delinsTC , LRG_311:g.99567_99568delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.787_788delinsTC ENSP00000514759.2:p.Lys263Ser
ENST00000710265.1:c.787_788delinsTC ENSP00000518161.1:p.Lys263Ser
ENST00000472832.3:c.787_788delinsTC ENSP00000483066.2:p.Lys263Ser
ENST00000688158.2:n.1522_1523delinsTC
ENST00000688922.2:c.*617_*618delinsTC ENSP00000508742.2:n.*617_*618delinsTC
ENST00000700021.1:c.742_743delinsTC ENSP00000514757.1:p.Lys248Ser
ENST00000700022.1:c.*126_*127delinsTC ENSP00000514758.1:n.*126_*127delinsTC
ENST00000700023.1:n.1945_1946delinsTC
ENST00000700024.1:n.2179_2180delinsTC
ENST00000700025.1:n.1556_1557delinsTC
ENST00000700026.1:n.424_425delinsTC
ENST00000700029.1:c.621_622delinsTC
ENST00000706954.1:c.787_788delinsTC ENSP00000516674.1:p.Lys263Ser
ENST00000706955.1:c.*822_*823delinsTC ENSP00000516675.1:n.*822_*823delinsTC
ENST00000686459.1:c.*373_*374delinsTC ENSP00000508909.1:n.*373_*374delinsTC
ENST00000688158.1:c.*898_*899delinsTC ENSP00000509254.1:n.*898_*899delinsTC
ENST00000688308.1:c.787_788delinsTC ENSP00000508752.1:p.Lys263Ser
ENST00000688922.1:c.708_709delinsTC
ENST00000693560.1:c.1306_1307delinsTC ENSP00000509861.1:p.Lys436Ser
ENST00000371953.8:c.787_788delinsTC MANE Select ENSP00000361021.3:p.Lys263Ser
ENST00000371953.7:c.787_788delinsTC ENSP00000361021.3:p.Lys263Ser
ENST00000472832.2:c.214_215delinsTC ENSP00000483066.1:p.Lys72Ser
NM_000314.5:c.787_788delinsTC NP_000305.3:p.Lys263Ser
NM_000314.6:c.787_788delinsTC NP_000305.3:p.Lys263Ser
NM_001304717.2:c.1306_1307delinsTC NP_001291646.2:p.Lys436Ser
NM_001304718.1:c.196_197delinsTC NP_001291647.1:p.Lys66Ser
XM_006717926.2:c.742_743delinsTC XP_006717989.1:p.Lys248Ser
XM_011539981.1:c.787_788delinsTC XP_011538283.1:p.Lys263Ser
XM_011539982.1:c.691_692delinsTC XP_011538284.1:p.Lys231Ser
XR_945791.1:n.1357_1358delinsTC
NM_000314.7:c.787_788delinsTC NP_000305.3:p.Lys263Ser
NM_001304717.5:c.1306_1307delinsTC NP_001291646.4:p.Lys436Ser
NM_001304718.2:c.196_197delinsTC NP_001291647.1:p.Lys66Ser
NM_000314.8:c.787_788delinsTC MANE Select NP_000305.3:p.Lys263Ser