Linked Data
MyVariant Identifiers:
chr17:g.4905830G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5002535G>T , CM000679.2:g.5002535G>T | GRCh38 |
| NC_000017.10:g.4905830G>T , CM000679.1:g.4905830G>T | GRCh37 |
| NC_000017.9:g.4846554G>T | NCBI36 |
| NG_034137.1:g.9588G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320785.10:c.501G>T (KIF1C) MANE Select | ENSP00000320821.5:p.Arg167= | |
| ENST00000320785.9:c.501G>T (KIF1C) | ENSP00000320821.5:p.Arg167= | |
| NM_006612.5:c.501G>T (KIF1C) | NP_006603.2:p.Arg167= | |
| XM_005256424.1:c.501G>T (KIF1C) | XP_005256481.1:p.Arg167= | |
| XM_005256424.2:c.501G>T (KIF1C) | XP_005256481.1:p.Arg167= | |
| XM_024450745.1:c.-39+3547C>A (INCA1) | XP_024306513.1:n.-39+3547C>A | |
| NM_006612.6:c.501G>T (KIF1C) MANE Select | NP_006603.2:p.Arg167= |