gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.71529785C>A , CM000685.2:g.71529785C>A | GRCh38 |
| NC_000023.10:g.70749635C>A , CM000685.1:g.70749635C>A | GRCh37 |
| NC_000023.9:g.70666360C>A | NCBI36 |
| NG_012771.2:g.168522C>A | |
| NG_015875.1:g.1724C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437147.8:c.1617C>A (TAF1) | ||
| ENST00000468167.6:n.1162C>A (TAF1) | ||
| ENST00000485087.6:c.1645C>A (TAF1) | ||
| ENST00000683668.1:c.5044C>A (TAF1) | ENSP00000507280.1:n.5044C>A | |
| ENST00000373775.8:c.1623C>A (TAF1) | ||
| ENST00000398297.2:n.441G>T (SOCS6P1) | ||
| ENST00000437147.7:c.1719C>A (TAF1) | ||
| ENST00000461764.5:n.1265C>A (TAF1) | ||
| ENST00000462588.5:n.1256C>A (TAF1) | ||
| ENST00000467309.5:n.584C>A (TAF1) | ||
| ENST00000468167.5:n.1191C>A (TAF1) | ||
| ENST00000485087.5:n.1163C>A (TAF1) | ||
| ENST00000497222.1:n.943C>A (TAF1) | ||
| NR_104387.1:n.5894C>A (TAF1) | ||
| NR_104388.1:n.5885C>A (TAF1) | ||
| NR_104389.1:n.5792C>A (TAF1) | ||
| NR_104390.1:n.5798C>A (TAF1) | ||
| NR_104391.1:n.5820C>A (TAF1) | ||
| NR_104392.1:n.5814C>A (TAF1) | ||
| NR_104393.1:n.5900C>A (TAF1) | ||
| NR_104394.1:n.5771C>A (TAF1) | ||
| NR_104395.1:n.5823C>A (TAF1) | ||
| NR_104396.1:n.1259C>A (TAF1) | ||
| NR_104387.2:n.5776C>A (TAF1) | ||
| NR_104388.2:n.5767C>A (TAF1) | ||
| NR_104389.2:n.5674C>A (TAF1) | ||
| NR_104390.2:n.5680C>A (TAF1) | ||
| NR_104391.2:n.5702C>A (TAF1) | ||
| NR_104392.2:n.5696C>A (TAF1) | ||
| NR_104393.2:n.5782C>A (TAF1) | ||
| NR_104394.2:n.5653C>A (TAF1) | ||
| NR_104395.2:n.5705C>A (TAF1) | ||
| NR_104396.2:n.805C>A (TAF1) |