Linked Data
gnomAD v4:
16-74713455-C-CGGAG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.74713457_74713458insAGGG , CM000678.2:g.74713457_74713458insAGGG | GRCh38 |
| NC_000016.9:g.74747355_74747356insAGGG , CM000678.1:g.74747355_74747356insAGGG | GRCh37 |
| NC_000016.8:g.73304856_73304857insAGGG | NCBI36 |
| NG_017070.1:g.66376_66377insCTCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219368.8:c.*734_*735insCTCC MANE Select | ENSP00000219368.3:n.*734_*735insCTCC | |
| ENST00000219368.7:c.*734_*735insCTCC | ENSP00000219368.3:n.*734_*735insCTCC | |
| ENST00000562145.1:n.1574_1575insCTCC | ||
| NM_024306.4:c.*734_*735insCTCC | NP_077282.3:n.*734_*735insCTCC | |
| XM_011523319.1:c.*734_*735insCTCC | XP_011521621.1:n.*734_*735insCTCC | |
| XM_011523319.2:c.*734_*735insCTCC | XP_011521621.1:n.*734_*735insCTCC | |
| NM_024306.5:c.*734_*735insCTCC MANE Select | NP_077282.3:n.*734_*735insCTCC |