Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5002639C= , CM000679.2:g.5002639C= | GRCh38 |
| NC_000017.10:g.4905934C= , CM000679.1:g.4905934C= | GRCh37 |
| NC_000017.9:g.4846658C= | NCBI36 |
| NG_034137.1:g.9692C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320785.10:c.605C= (KIF1C) MANE Select | ENSP00000320821.5:p.Ala202= | |
| ENST00000320785.9:c.605C= (KIF1C) | ENSP00000320821.5:p.Ala202= | |
| NM_006612.5:c.605C= (KIF1C) | NP_006603.2:p.Ala202= | |
| XM_005256424.1:c.605C= (KIF1C) | XP_005256481.1:p.Ala202= | |
| XM_005256424.2:c.605C= (KIF1C) | XP_005256481.1:p.Ala202= | |
| XM_024450745.1:c.-39+3443G= (INCA1) | XP_024306513.1:n.-39+3443G= | |
| NM_006612.6:c.605C= (KIF1C) MANE Select | NP_006603.2:p.Ala202= |