Canonical Allele Identifier: CA684581059

Linked Data

dbSNP Id: rs536364664

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175170_122175181dup , CM000674.2:g.122175170_122175181dup GRCh38
NC_000012.11:g.122659717_122659728dup , CM000674.1:g.122659717_122659728dup GRCh37
NC_000012.10:g.121225670_121225681dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7388_-406+7399dup (LRRC43) ENSP00000438751.1:n.-406+7388_-406+7399dup
NM_152759.4:c.-406+7388_-406+7399dup (LRRC43) NP_689972.3:n.-406+7388_-406+7399dup
XM_011538326.1:c.-65-929_-65-918dup (IL31) XP_011536628.1:n.-65-929_-65-918dup
NM_152759.5:c.-406+7388_-406+7399dup (LRRC43) NP_689972.3:n.-406+7388_-406+7399dup