Canonical Allele Identifier: CA2068251786

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175178_122175182delinsCTTTT , CM000674.2:g.122175178_122175182delinsCTTTT GRCh38
NC_000012.11:g.122659725_122659729delinsCTTTT , CM000674.1:g.122659725_122659729delinsCTTTT GRCh37
NC_000012.10:g.121225678_121225682delinsCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7396_-406+7400delinsCTTTT (LRRC43) ENSP00000438751.1:n.-406+7396_-406+7400delinsCTTTT
NM_152759.4:c.-406+7396_-406+7400delinsCTTTT (LRRC43) NP_689972.3:n.-406+7396_-406+7400delinsCTTTT
XM_011538326.1:c.-65-945_-65-941delinsAAAAG (IL31) XP_011536628.1:n.-65-945_-65-941delinsAAAAG
NM_152759.5:c.-406+7396_-406+7400delinsCTTTT (LRRC43) NP_689972.3:n.-406+7396_-406+7400delinsCTTTT