Linked Data
dbSNP Id:
rs1953526288
gnomAD v3:
12-122175162-C-CTTTCTTTA
gnomAD v4:
12-122175162-C-CTTTCTTTA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.122175169_122175170insATTTCTTT , CM000674.2:g.122175169_122175170insATTTCTTT | GRCh38 |
| NC_000012.11:g.122659716_122659717insATTTCTTT , CM000674.1:g.122659716_122659717insATTTCTTT | GRCh37 |
| NC_000012.10:g.121225669_121225670insATTTCTTT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537729.5:c.-406+7387_-406+7388insATTTCTTT (LRRC43) | ENSP00000438751.1:n.-406+7387_-406+7388insATTTCTTT | |
| NM_152759.4:c.-406+7387_-406+7388insATTTCTTT (LRRC43) | NP_689972.3:n.-406+7387_-406+7388insATTTCTTT | |
| XM_011538326.1:c.-65-926_-65-925insTAAAGAAA (IL31) | XP_011536628.1:n.-65-926_-65-925insTAAAGAAA | |
| NM_152759.5:c.-406+7387_-406+7388insATTTCTTT (LRRC43) | NP_689972.3:n.-406+7387_-406+7388insATTTCTTT |