Canonical Allele Identifier: CA684581658

Linked Data

dbSNP Id: rs1212809154

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176179_122176182del , CM000674.2:g.122176179_122176182del GRCh38
NC_000012.11:g.122660726_122660729del , CM000674.1:g.122660726_122660729del GRCh37
NC_000012.10:g.121226679_121226682del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-405-8340_-405-8337del (LRRC43) ENSP00000438751.1:n.-405-8340_-405-8337de...
NM_152759.4:c.-405-8340_-405-8337del (LRRC43) NP_689972.3:n.-405-8340_-405-8337del
XM_011538326.1:c.-65-1942_-65-1939del (IL31) XP_011536628.1:n.-65-1942_-65-1939del
NM_152759.5:c.-405-8340_-405-8337del (LRRC43) NP_689972.3:n.-405-8340_-405-8337del