Canonical Allele Identifier: CA2607410561

Linked Data

dbSNP Id: rs2105937576

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216033983del , CM000664.2:g.216033983del GRCh38
NC_000002.11:g.216898706del , CM000664.1:g.216898706del GRCh37
NC_000002.10:g.216606951del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424992.5:c.-88del (MREG) ENSP00000413302.1:n.-88del
ENST00000442122.5:c.*440+5209del (PECR) ENSP00000395512.1:n.*440+5209del
XR_001738847.2:n.1056-1130del (PECR)
NM_001372189.1:c.-88del (MREG) NP_001359118.1:n.-88del