Canonical Allele Identifier: CA2610046009

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863374del , CM000672.2:g.87863374del GRCh38
NC_000010.10:g.89623131del , CM000672.1:g.89623131del GRCh37
NC_000010.9:g.89613111del NCBI36
NG_007466.2:g.4937del , LRG_311:g.4937del
NG_033079.1:g.5067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+732del (PTEN) ENSP00000516674.1:n.-17+732del
ENST00000688308.1:c.-17+261del (PTEN) ENSP00000508752.1:n.-17+261del
ENST00000445946.5:c.-884del (KLLN) MANE Select ENSP00000392204.2:n.-884del
ENST00000371953.7:c.-1096del (PTEN) ENSP00000361021.3:n.-1096del
ENST00000445946.3:c.-884del (KLLN) ENSP00000392204.2:n.-884del
NM_001126049.1:c.-884del (KLLN) NP_001119521.1:n.-884del
NM_001126049.2:c.-884del (KLLN) MANE Select NP_001119521.1:n.-884del