Canonical Allele Identifier: CA1042294309

Linked Data

dbSNP Id: rs1694748399

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033782_216033788del , CM000664.2:g.216033782_216033788del GRCh38
NC_000002.11:g.216898505_216898511del , CM000664.1:g.216898505_216898511del GRCh37
NC_000002.10:g.216606750_216606756del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424992.5:c.-68+176_-68+182del (MREG) ENSP00000413302.1:n.-68+176_-68+182del
ENST00000439791.5:c.-171_-165del (MREG) ENSP00000411076.1:n.-171_-165del
ENST00000442122.5:c.*440+5405_*440+5411del (PECR) ENSP00000395512.1:n.*440+5405_*440+5411del
XR_001738847.2:n.1056-934_1056-928del (PECR)
NM_001372189.1:c.-68+176_-68+182del (MREG) NP_001359118.1:n.-68+176_-68+182del
NM_001372190.1:c.-171_-165del (MREG) NP_001359119.1:n.-171_-165del