Linked Data
gnomAD v4:
21-45990499-CGTGAAGGTGACCCG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990501_45990514del , CM000683.2:g.45990501_45990514del | GRCh38 |
| NC_000021.8:g.47410415_47410428del , CM000683.1:g.47410415_47410428del | GRCh37 |
| NC_000021.7:g.46234843_46234856del | NCBI36 |
| NG_008674.1:g.13753_13766del , LRG_475:g.13753_13766del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+79_1002+92del MANE Select | ENSP00000355180.3:n.1002+79_1002+92del | |
| ENST00000361866.7:c.1002+79_1002+92del | ENSP00000355180.3:n.1002+79_1002+92del | |
| ENST00000612273.1:c.1002+79_1002+92del | ENSP00000483630.1:n.1002+79_1002+92del | |
| NM_001848.2:c.1002+79_1002+92del , LRG_475t1:c.1002+79_1002+92del | NP_001839.2:n.1002+79_1002+92del | |
| NM_001848.3:c.1002+79_1002+92del MANE Select | NP_001839.2:n.1002+79_1002+92del |