Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107661611T>C , CM000669.2:g.107661611T>C | GRCh38 |
| NC_000007.13:g.107302056T>C , CM000669.1:g.107302056T>C | GRCh37 |
| NC_000007.12:g.107089292T>C | NCBI36 |
| NG_008489.1:g.5977T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644269.2:c.-3-28T>C (SLC26A4) MANE Select | ENSP00000494017.1:n.-3-28T>C | |
| ENST00000265715.7:c.-3-28T>C (SLC26A4) | ENSP00000265715.3:n.-3-28T>C | |
| ENST00000440056.1:c.-3-28T>C (SLC26A4) | ENSP00000394760.1:n.-3-28T>C | |
| NM_000441.1:c.-3-28T>C (SLC26A4) | NP_000432.1:n.-3-28T>C | |
| NR_028137.1:n.188A>G (SLC26A4-AS1) | ||
| XM_005250425.1:c.-3-28T>C (SLC26A4) | XP_005250482.1:n.-3-28T>C | |
| XM_005250425.2:c.-3-28T>C (SLC26A4) | XP_005250482.1:n.-3-28T>C | |
| NM_000441.2:c.-3-28T>C (SLC26A4) MANE Select | NP_000432.1:n.-3-28T>C |