Canonical Allele Identifier: CA1926142916

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863356T= , CM000672.2:g.87863356T= GRCh38
NC_000010.10:g.89623113T= , CM000672.1:g.89623113T= GRCh37
NC_000010.9:g.89613093T= NCBI36
NG_007466.2:g.4919T= , LRG_311:g.4919T=
NG_033079.1:g.5082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+714T= (PTEN) ENSP00000516674.1:n.-17+714T=
ENST00000688308.1:c.-17+243T= (PTEN) ENSP00000508752.1:n.-17+243T=
ENST00000445946.5:c.-869A= (KLLN) MANE Select ENSP00000392204.2:n.-869A=
ENST00000371953.7:c.-1114T= (PTEN) ENSP00000361021.3:n.-1114T=
ENST00000445946.3:c.-869A= (KLLN) ENSP00000392204.2:n.-869A=
NM_001126049.1:c.-869A= (KLLN) NP_001119521.1:n.-869A=
NM_001126049.2:c.-869A= (KLLN) MANE Select NP_001119521.1:n.-869A=