Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659093T>C , CM000685.2:g.136659093T>C | GRCh38 |
| NC_000023.10:g.135741252T>C , CM000685.1:g.135741252T>C | GRCh37 |
| NC_000023.9:g.135568918T>C | NCBI36 |
| NG_007280.1:g.15917T>C , LRG_141:g.15917T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695724.1:c.*82T>C | ENSP00000512122.1:n.*82T>C | |
| ENST00000695725.1:c.*19T>C | ENSP00000512123.1:n.*19T>C | |
| ENST00000695726.1:n.2432T>C | ||
| ENST00000695729.1:n.3267T>C | ||
| ENST00000370629.7:c.464T>C MANE Select | ENSP00000359663.2:p.Leu155Pro | |
| ENST00000370628.2:c.401T>C | ENSP00000359662.2:p.Leu134Pro | |
| ENST00000370629.6:c.464T>C | ENSP00000359663.2:p.Leu155Pro | |
| NM_000074.2:c.464T>C , LRG_141t1:c.464T>C | NP_000065.1:p.Leu155Pro | |
| NM_000074.3:c.464T>C MANE Select | NP_000065.1:p.Leu155Pro |