Linked Data
gnomAD v4:
1-55063609-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55063613dup , CM000663.2:g.55063613dup | GRCh38 |
| NC_000001.10:g.55529286dup , CM000663.1:g.55529286dup | GRCh37 |
| NC_000001.9:g.55301874dup | NCBI36 |
| NG_009061.1:g.29067dup , LRG_275:g.29067dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*448dup | ENSP00000501161.2:n.*448dup | |
| ENST00000710286.1:c.*29dup | ENSP00000518176.1:n.*29dup | |
| ENST00000673903.1:c.*29dup | ENSP00000501257.1:n.*29dup | |
| ENST00000302118.5:c.*29dup MANE Select | ENSP00000303208.5:n.*29dup | |
| ENST00000490692.1:n.2654dup | ||
| NM_174936.3:c.*29dup , LRG_275t1:c.*29dup | NP_777596.2:n.*29dup | |
| NR_110451.1:n.1715dup | ||
| XM_011541193.1:c.*29dup | XP_011539495.1:n.*29dup | |
| NM_174936.4:c.*29dup MANE Select | NP_777596.2:n.*29dup | |
| NR_110451.2:n.1715dup |