Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189414_20189415delinsCA , CM000675.2:g.20189414_20189415delinsCA | GRCh38 |
| NC_000013.10:g.20763553_20763554delinsCA , CM000675.1:g.20763553_20763554delinsCA | GRCh37 |
| NC_000013.9:g.19661553_19661554delinsCA | NCBI36 |
| NG_008358.1:g.8561_8562delinsTG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382844.2:c.167_168delinsTG | ENSP00000372295.1:p.Leu56= | |
| ENST00000382848.5:c.167_168delinsTG MANE Select | ENSP00000372299.4:p.Leu56= | |
| ENST00000382844.1:c.167_168delinsTG | ENSP00000372295.1:p.Leu56= | |
| ENST00000382848.4:c.167_168delinsTG | ENSP00000372299.4:p.Leu56= | |
| NM_004004.5:c.167_168delinsTG | NP_003995.2:p.Leu56= | |
| XM_011535049.1:c.167_168delinsTG | XP_011533351.1:p.Leu56= | |
| XM_011535049.2:c.167_168delinsTG | XP_011533351.1:p.Leu56= | |
| NM_004004.6:c.167_168delinsTG MANE Select | NP_003995.2:p.Leu56= |