Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2340618G>A , CM000678.2:g.2340618G>A | GRCh38 |
| NC_000016.9:g.2390619G>A , CM000678.1:g.2390619G>A | GRCh37 |
| NC_000016.8:g.2330620G>A | NCBI36 |
| NG_011790.1:g.5129C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301732.10:c.-584C>T (ABCA3) MANE Select | ENSP00000301732.5:n.-584C>T | |
| ENST00000640929.1:n.42+1287G>A (ABCA17P) | ||
| ENST00000301732.9:c.-584C>T (ABCA3) | ENSP00000301732.5:n.-584C>T | |
| ENST00000382381.7:c.-584C>T (ABCA3) | ENSP00000371818.3:n.-584C>T | |
| ENST00000512848.5:n.182+1287G>A (ABCA17P) | ||
| NM_001089.2:c.-584C>T (ABCA3) | NP_001080.2:n.-584C>T | |
| NM_001089.3:c.-584C>T (ABCA3) MANE Select | NP_001080.2:n.-584C>T |