Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91273415A>G , CM000676.2:g.91273415A>G | GRCh38 |
| NC_000014.8:g.91739759A>G , CM000676.1:g.91739759A>G | GRCh37 |
| NC_000014.7:g.90809512A>G | NCBI36 |
| NG_033118.1:g.149430T>C | |
| NG_033118.2:g.149430T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5297T>C MANE Select | ENSP00000374507.6:p.Val1766Ala | |
| ENST00000331194.8:c.869T>C | ENSP00000330332.8:p.Val290Ala | |
| ENST00000389857.10:c.5297T>C | ENSP00000374507.6:p.Val1766Ala | |
| ENST00000556726.5:c.1525T>C | ||
| NM_001080414.3:c.5297T>C | NP_001073883.2:p.Val1766Ala | |
| XM_011536796.1:c.5189T>C | XP_011535098.1:p.Val1730Ala | |
| XM_011536796.2:c.5189T>C | XP_011535098.1:p.Val1730Ala | |
| XM_017021336.1:c.2378T>C | XP_016876825.1:p.Val793Ala | |
| NM_001080414.4:c.5297T>C MANE Select | NP_001073883.2:p.Val1766Ala |