dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.10372766G>T , CM000674.2:g.10372766G>T | GRCh38 |
| NC_000012.11:g.10525365G>T , CM000674.1:g.10525365G>T | GRCh37 |
| NC_000012.10:g.10416632G>T | NCBI36 |
| NG_027762.1:g.22276C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240618.11:c.*348C>A (KLRK1) MANE Select | ENSP00000240618.6:n.*348C>A | |
| ENST00000240618.10:c.*348C>A (KLRK1) | ENSP00000240618.6:n.*348C>A | |
| ENST00000540267.5:n.1437C>A (KLRK1) | ||
| ENST00000543572.6:c.1337C>A (KLRC4-KLRK1) | ENSP00000456286.1:n.1337C>A | |
| NM_001199805.1:c.*348C>A (KLRC4-KLRK1) | NP_001186734.1:n.*348C>A | |
| NM_007360.3:c.*348C>A (KLRK1) | NP_031386.2:n.*348C>A | |
| NR_120430.1:n.266-1269G>T (KLRK1-AS1) | ||
| NM_007360.4:c.*348C>A (KLRK1) MANE Select | NP_031386.2:n.*348C>A |