Canonical Allele Identifier: CA952666786

Linked Data

dbSNP Id: rs1284137195

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175184_122175187dup , CM000674.2:g.122175184_122175187dup GRCh38
NC_000012.11:g.122659731_122659734dup , CM000674.1:g.122659731_122659734dup GRCh37
NC_000012.10:g.121225684_121225687dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7402_-406+7405dup (LRRC43) ENSP00000438751.1:n.-406+7402_-406+7405dup
NM_152759.4:c.-406+7402_-406+7405dup (LRRC43) NP_689972.3:n.-406+7402_-406+7405dup
XM_011538326.1:c.-65-945_-65-942dup (IL31) XP_011536628.1:n.-65-945_-65-942dup
NM_152759.5:c.-406+7402_-406+7405dup (LRRC43) NP_689972.3:n.-406+7402_-406+7405dup