Canonical Allele Identifier: CA1926177030
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967618_87967621delinsATTG , CM000672.2:g.87967618_87967621delinsATTG GRCh38
NC_000010.10:g.89727375_89727378delinsATTG , CM000672.1:g.89727375_89727378delinsATTG GRCh37
NC_000010.9:g.89717355_89717358delinsATTG NCBI36
NG_007466.2:g.109180_109183delinsATTG , LRG_311:g.109180_109183delinsATTG

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2387_*2390delinsATTG ENSP00000518161.1:n.*2387_*2390delinsATTG...
ENST00000688158.2:n.4093_4096delinsATTG
ENST00000706954.1:c.*2146_*2149delinsATTG ENSP00000516674.1:n.*2146_*2149delinsATTG...
ENST00000706955.1:c.*3393_*3396delinsATTG ENSP00000516675.1:n.*3393_*3396delinsATTG...
ENST00000688158.1:c.*3469_*3472delinsATTG ENSP00000509254.1:n.*3469_*3472delinsATTG...
ENST00000693560.1:c.*2146_*2149delinsATTG ENSP00000509861.1:n.*2146_*2149delinsATTG...
ENST00000371953.8:c.*2146_*2149delinsATTG MANE Select ENSP00000361021.3:n.*2146_*2149delinsATTG...
ENST00000371953.7:c.*2146_*2149delinsATTG ENSP00000361021.3:n.*2146_*2149delinsATTG...
NM_000314.5:c.*2146_*2149delinsATTG NP_000305.3:n.*2146_*2149delinsATTG
NM_000314.6:c.*2146_*2149delinsATTG NP_000305.3:n.*2146_*2149delinsATTG
NM_001304717.2:c.*2146_*2149delinsATTG NP_001291646.2:n.*2146_*2149delinsATTG
NM_001304718.1:c.*2146_*2149delinsATTG NP_001291647.1:n.*2146_*2149delinsATTG
XM_006717926.2:c.*2146_*2149delinsATTG XP_006717989.1:n.*2146_*2149delinsATTG
XM_011539982.1:c.*2146_*2149delinsATTG XP_011538284.1:n.*2146_*2149delinsATTG
XR_945791.1:n.3928_3931delinsATTG
NM_000314.7:c.*2146_*2149delinsATTG NP_000305.3:n.*2146_*2149delinsATTG
NM_001304717.5:c.*2146_*2149delinsATTG NP_001291646.4:n.*2146_*2149delinsATTG
NM_001304718.2:c.*2146_*2149delinsATTG NP_001291647.1:n.*2146_*2149delinsATTG
NM_000314.8:c.*2146_*2149delinsATTG MANE Select NP_000305.3:n.*2146_*2149delinsATTG