Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5004858T>C , CM000679.2:g.5004858T>C | GRCh38 |
| NC_000017.10:g.4908153T>C , CM000679.1:g.4908153T>C | GRCh37 |
| NC_000017.9:g.4848877T>C | NCBI36 |
| NG_034137.1:g.11911T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006612.6:c.1023T>C (KIF1C) MANE Select | NP_006603.2:p.Tyr341= |
| ENST00000320785.10:c.1023T>C (KIF1C) MANE Select | ENSP00000320821.5:p.Tyr341= |
| NM_006612.5:c.1023T>C (KIF1C) | NP_006603.2:p.Tyr341= |
| ENST00000320785.9:c.1023T>C (KIF1C) | ENSP00000320821.5:p.Tyr341= |
| XM_005256424.1:c.1023T>C (KIF1C) | XP_005256481.1:p.Tyr341= |
| XM_005256424.2:c.1023T>C (KIF1C) | XP_005256481.1:p.Tyr341= |
| XM_024450745.1:c.-39+1224A>G (INCA1) | XP_024306513.1:n.-39+1224A>G |