Canonical Allele Identifier: CA2068251842

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175238C= , CM000674.2:g.122175238C= GRCh38
NC_000012.11:g.122659785C= , CM000674.1:g.122659785C= GRCh37
NC_000012.10:g.121225738C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_152759.4:c.-406+7456C= (LRRC43) NP_689972.3:n.-406+7456C=
NM_152759.5:c.-406+7456C= (LRRC43) NP_689972.3:n.-406+7456C=
ENST00000537729.5:c.-406+7456C= (LRRC43) ENSP00000438751.1:n.-406+7456C=
XM_011538326.1:c.-65-1001G= (IL31) XP_011536628.1:n.-65-1001G=