Canonical Allele Identifier: CA607946140

Linked Data

dbSNP Id: rs536364664

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175181_122175182insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT , CM000674.2:g.122175181_122175182insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT GRCh38
NC_000012.11:g.122659728_122659729insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT , CM000674.1:g.122659728_122659729insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT GRCh37
NC_000012.10:g.121225681_121225682insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT (LRRC43) ENSP00000438751.1:n.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTT...
NM_152759.4:c.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT (LRRC43) NP_689972.3:n.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTTTCTTTC...
XM_011538326.1:c.-65-918_-65-917insGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA (IL31) XP_011536628.1:n.-65-918_-65-917insGAAAGAAAGAAAGAAAGAAAGAAAGA...
NM_152759.5:c.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT (LRRC43) NP_689972.3:n.-406+7399_-406+7400insCTTTCTTTCTTTCTTTCTTTCTTTC...