Canonical Allele Identifier: CA916773659

Linked Data

dbSNP Id: rs1574668956

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033761_216033762del , CM000664.2:g.216033761_216033762del GRCh38
NC_000002.11:g.216898484_216898485del , CM000664.1:g.216898484_216898485del GRCh37
NC_000002.10:g.216606729_216606730del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424992.5:c.-68+202_-68+203del (MREG) ENSP00000413302.1:n.-68+202_-68+203del
ENST00000439791.5:c.-145_-144del (MREG) ENSP00000411076.1:n.-145_-144del
ENST00000442122.5:c.*440+5431_*440+5432del (PECR) ENSP00000395512.1:n.*440+5431_*440+5432del
XR_001738847.2:n.1056-908_1056-907del (PECR)
NM_001372189.1:c.-68+202_-68+203del (MREG) NP_001359118.1:n.-68+202_-68+203del
NM_001372190.1:c.-145_-144del (MREG) NP_001359119.1:n.-145_-144del