Linked Data
gnomAD v2:
19-15651436-CGGCGG-C
gnomAD v4:
19-15540625-CGGCGG-C
MyVariant Identifiers:
chr19:g.15651437_15651441del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15540627_15540631del , CM000681.2:g.15540627_15540631del | GRCh38 |
| NC_000019.9:g.15651438_15651442del , CM000681.1:g.15651438_15651442del | GRCh37 |
| NC_000019.8:g.15512438_15512442del | NCBI36 |
| NG_007987.1:g.37103_37107del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269703.8:c.849_853del MANE Select | ENSP00000269703.1:p.Arg284ThrfsTer11 | |
| ENST00000269703.7:c.849_853del | ENSP00000269703.1:p.Arg284ThrfsTer11 | |
| ENST00000601005.2:c.849_853del | ENSP00000469866.1:p.Arg284ThrfsTer11 | |
| NM_173483.3:c.849_853del | NP_775754.2:p.Arg284ThrfsTer11 | |
| XM_011527692.1:c.849_853del | XP_011525994.1:p.Arg284ThrfsTer11 | |
| XM_011527693.1:c.849_853del | XP_011525995.1:p.Arg284ThrfsTer11 | |
| XM_011527692.2:c.849_853del | XP_011525994.1:p.Arg284ThrfsTer11 | |
| XM_011527693.2:c.849_853del | XP_011525995.1:p.Arg284ThrfsTer11 | |
| NM_173483.4:c.849_853del MANE Select | NP_775754.2:p.Arg284ThrfsTer11 |