Canonical Allele Identifier: CA684581116
Gene: LRRC43 HGNC NCBI
IL31 HGNC NCBI

Linked Data

dbSNP Id: rs1464808413
gnomAD v3: 12-122175178-C-CTTTCT
gnomAD v4: 12-122175178-C-CTTTCT
MyVariant Identifiers: chr12:g.122659725_122659726insTTTCT (hg19) chr12:g.122175178_122175179insTTTCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175181_122175182insCTTTT , CM000674.2:g.122175181_122175182insCTTTT GRCh38
NC_000012.11:g.122659728_122659729insCTTTT , CM000674.1:g.122659728_122659729insCTTTT GRCh37
NC_000012.10:g.121225681_121225682insCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7399_-406+7400insCTTTT (LRRC43) ENSP00000438751.1:n.-406+7399_-406+7400insCTTTT
NM_152759.4:c.-406+7399_-406+7400insCTTTT (LRRC43) NP_689972.3:n.-406+7399_-406+7400insCTTTT
XM_011538326.1:c.-65-942_-65-941insAGAAA (IL31) XP_011536628.1:n.-65-942_-65-941insAGAAA
NM_152759.5:c.-406+7399_-406+7400insCTTTT (LRRC43) NP_689972.3:n.-406+7399_-406+7400insCTTTT
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