Canonical Allele Identifier: CA244719612

Linked Data

dbSNP Id: rs919022318

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175044del , CM000674.2:g.122175044del GRCh38
NC_000012.11:g.122659591del , CM000674.1:g.122659591del GRCh37
NC_000012.10:g.121225544del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7262del (LRRC43) ENSP00000438751.1:n.-406+7262del
NM_152759.4:c.-406+7262del (LRRC43) NP_689972.3:n.-406+7262del
XM_011538326.1:c.-65-806del (IL31) XP_011536628.1:n.-65-806del
NM_152759.5:c.-406+7262del (LRRC43) NP_689972.3:n.-406+7262del