Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5020033A>T , CM000679.2:g.5020033A>T | GRCh38 |
| NC_000017.10:g.4923328A>T , CM000679.1:g.4923328A>T | GRCh37 |
| NC_000017.9:g.4864052A>T | NCBI36 |
| NG_034137.1:g.27086A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006612.6:c.1704A>T (KIF1C) MANE Select | NP_006603.2:p.Thr568= |
| ENST00000320785.10:c.1704A>T (KIF1C) MANE Select | ENSP00000320821.5:p.Thr568= |
| NM_006612.5:c.1704A>T (KIF1C) | NP_006603.2:p.Thr568= |
| NR_120665.1:n.61T>A (KIF1C-AS1) | |
| NR_120665.2:n.61T>A (KIF1C-AS1) | |
| ENST00000320785.9:c.1704A>T (KIF1C) | ENSP00000320821.5:p.Thr568= |
| ENST00000573815.1:n.246A>T (KIF1C) | |
| XM_005256424.1:c.1704A>T (KIF1C) | XP_005256481.1:p.Thr568= |
| XM_005256424.2:c.1704A>T (KIF1C) | XP_005256481.1:p.Thr568= |