Linked Data
gnomAD v2:
11-47372740-GC-G
gnomAD v4:
11-47351189-GC-G
MyVariant Identifiers:
chr11:g.47372741del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47351193del , CM000673.2:g.47351193del | GRCh38 |
| NC_000011.9:g.47372744del , CM000673.1:g.47372744del | GRCh37 |
| NC_000011.8:g.47329320del | NCBI36 |
| NG_007667.1:g.6513del , LRG_386:g.6513del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.292+49del MANE Select | ENSP00000442795.1:n.292+49del | |
| ENST00000256993.8:c.292+49del | ENSP00000256993.5:n.292+49del | |
| ENST00000399249.6:c.292+49del | ENSP00000382193.2:n.292+49del | |
| ENST00000544791.1:c.292+49del | ENSP00000444259.1:n.292+49del | |
| ENST00000545968.5:c.292+49del | ENSP00000442795.1:n.292+49del | |
| NM_000256.3:c.292+49del , LRG_386t1:c.292+49del MANE Select | NP_000247.2:n.292+49del | |
| XM_011520117.1:c.292+49del | XP_011518419.1:n.292+49del | |
| XM_011520118.1:c.292+49del | XP_011518420.1:n.292+49del |