Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43039603G= , CM000684.2:g.43039603G= | GRCh38 |
| NC_000022.10:g.43435609G= , CM000684.1:g.43435609G= | GRCh37 |
| NC_000022.9:g.41765553G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012263.5:c.*173C= (TTLL1) MANE Select | NP_036395.1:n.*173C= |
| ENST00000266254.12:c.*173C= (TTLL1) MANE Select | ENSP00000266254.7:n.*173C= |
| NM_012263.4:c.*173C= (TTLL1) | NP_036395.1:n.*173C= |
| NR_027779.1:n.1790C= (TTLL1) | |
| NR_027779.2:n.1753C= (TTLL1) | |
| NR_125362.1:n.1019G= (TTLL1-AS1) |