Linked Data
gnomAD v4:
11-55811764-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55811766del , CM000673.2:g.55811766del | GRCh38 |
| NC_000011.9:g.55579242del , CM000673.1:g.55579242del | GRCh37 |
| NC_000011.8:g.55335818del | NCBI36 |
| NG_052620.1:g.5400del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.300del MANE Select | ENSP00000485319.1:p.Gln100HisfsTer18 | |
| ENST00000333973.3:c.300del | ENSP00000335529.2:p.Gln100HisfsTer18 | |
| ENST00000623450.1:c.300del | ENSP00000485509.1:p.Gln100HisfsTer18 | |
| ENST00000625203.1:c.300del | ENSP00000485319.1:p.Gln100HisfsTer18 | |
| NM_001004738.1:c.300del | NP_001004738.1:p.Gln100HisfsTer18 | |
| NM_001004738.2:c.300del MANE Select | NP_001004738.1:p.Gln100HisfsTer18 |