Canonical Allele Identifier: CA2610045698

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863172del , CM000672.2:g.87863172del GRCh38
NC_000010.10:g.89622929del , CM000672.1:g.89622929del GRCh37
NC_000010.9:g.89612909del NCBI36
NG_007466.2:g.4735del , LRG_311:g.4735del
NG_033079.1:g.5266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+530del (PTEN) ENSP00000516674.1:n.-17+530del
ENST00000688308.1:c.-17+59del (PTEN) ENSP00000508752.1:n.-17+59del
ENST00000445946.5:c.-685del (KLLN) MANE Select ENSP00000392204.2:n.-685del
ENST00000371953.7:c.-1298del (PTEN) ENSP00000361021.3:n.-1298del
ENST00000445946.3:c.-685del (KLLN) ENSP00000392204.2:n.-685del
NM_001126049.1:c.-685del (KLLN) NP_001119521.1:n.-685del
NM_001126049.2:c.-685del (KLLN) MANE Select NP_001119521.1:n.-685del