Linked Data
ClinVar Variation Id:
454658
ClinVar RCV Id:
RCV000552871
dbSNP Id:
rs1261703349
gnomAD v4:
7-21901024-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21901024C>T , CM000669.2:g.21901024C>T | GRCh38 |
| NC_000007.13:g.21940642C>T , CM000669.1:g.21940642C>T | GRCh37 |
| NC_000007.12:g.21907167C>T | NCBI36 |
| NG_012886.2:g.362810C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000406877.8:c.*1298G>A (CDCA7L) MANE Select | ENSP00000383986.3:n.*1298G>A | |
| ENST00000409508.8:c.13321C>T (DNAH11) MANE Select | ENSP00000475939.1:p.Gln4441Ter | |
| ENST00000328843.10:c.13342C>T (DNAH11) | ENSP00000330671.7:p.Gln4448Ter | |
| ENST00000356195.9:c.*1298G>A (CDCA7L) | ENSP00000348523.5:n.*1298G>A | |
| ENST00000406877.7:c.*1298G>A (CDCA7L) | ENSP00000383986.3:n.*1298G>A | |
| ENST00000409508.7:c.13321C>T (DNAH11) | ENSP00000475939.1:p.Gln4441Ter | |
| ENST00000479878.1:n.692C>T (DNAH11) | ||
| ENST00000488845.1:n.1820G>A (CDCA7L) | ||
| ENST00000620169.4:c.13342C>T (DNAH11) | ENSP00000481693.1:p.Gln4448Ter | |
| NM_001127370.2:c.*1298G>A (CDCA7L) | NP_001120842.1:n.*1298G>A | |
| NM_001127371.2:c.*1298G>A (CDCA7L) | NP_001120843.1:n.*1298G>A | |
| NM_001277115.1:c.13321C>T (DNAH11) | NP_001264044.1:p.Gln4441Ter | |
| NM_018719.4:c.*1298G>A (CDCA7L) | NP_061189.2:n.*1298G>A | |
| NM_001277115.2:c.13321C>T (DNAH11) MANE Select | NP_001264044.1:p.Gln4441Ter | |
| NM_018719.5:c.*1298G>A (CDCA7L) MANE Select | NP_061189.2:n.*1298G>A | |
| NM_001127370.3:c.*1298G>A (CDCA7L) | NP_001120842.1:n.*1298G>A | |
| NM_001127371.3:c.*1298G>A (CDCA7L) | NP_001120843.1:n.*1298G>A |