Canonical Allele Identifier: CA1327642322

Linked Data

dbSNP Id: rs1694639250

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216028967_216028968del , CM000664.2:g.216028967_216028968del GRCh38
NC_000002.11:g.216893690_216893691del , CM000664.1:g.216893690_216893691del GRCh37
NC_000002.10:g.216601935_216601936del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420348.1:c.-68+3824_-68+3825del (MREG) ENSP00000404470.1:n.-68+3824_-68+3825del
ENST00000424992.5:c.-68+4997_-68+4998del (MREG) ENSP00000413302.1:n.-68+4997_-68+4998del
ENST00000439791.5:c.-68+4718_-68+4719del (MREG) ENSP00000411076.1:n.-68+4718_-68+4719del
ENST00000442122.5:c.*440+10226_*440+10227del (PECR) ENSP00000395512.1:n.*440+10226_*440+10227del
NM_001372189.1:c.-68+4997_-68+4998del (MREG) NP_001359118.1:n.-68+4997_-68+4998del
NM_001372190.1:c.-68+4718_-68+4719del (MREG) NP_001359119.1:n.-68+4718_-68+4719del