Canonical Allele Identifier: CA607946138
Gene: LRRC43 HGNC NCBI
IL31 HGNC NCBI

Linked Data

dbSNP Id: rs536364664
gnomAD v2: 12-122659701-TTTTCTTTCTTTC-T
gnomAD v3: 12-122175154-TTTTCTTTCTTTC-T
gnomAD v4: 12-122175154-TTTTCTTTCTTTC-T
MyVariant Identifiers: chr12:g.122659702_122659713del (hg19) chr12:g.122175155_122175166del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175170_122175181del , CM000674.2:g.122175170_122175181del GRCh38
NC_000012.11:g.122659717_122659728del , CM000674.1:g.122659717_122659728del GRCh37
NC_000012.10:g.121225670_121225681del NCBI36

Transcript Alleles

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