Canonical Allele Identifier: CA2068251898

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175286C= , CM000674.2:g.122175286C= GRCh38
NC_000012.11:g.122659833C= , CM000674.1:g.122659833C= GRCh37
NC_000012.10:g.121225786C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7504C= (LRRC43) ENSP00000438751.1:n.-406+7504C=
NM_152759.4:c.-406+7504C= (LRRC43) NP_689972.3:n.-406+7504C=
XM_011538326.1:c.-65-1049G= (IL31) XP_011536628.1:n.-65-1049G=
NM_152759.5:c.-406+7504C= (LRRC43) NP_689972.3:n.-406+7504C=