Linked Data
gnomAD v4:
5-159315899-C-CAA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159315899_159315900insAA , CM000667.2:g.159315899_159315900insAA | GRCh38 |
| NC_000005.9:g.158742907_158742908insAA , CM000667.1:g.158742907_158742908insAA | GRCh37 |
| NC_000005.8:g.158675485_158675486insAA | NCBI36 |
| NG_009618.1:g.19574_19575insTT , LRG_71:g.19574_19575insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696750.1:c.*201_*202insTT | ENSP00000512849.1:n.*201_*202insTT | |
| ENST00000696751.1:c.*683_*684insTT | ENSP00000512850.1:n.*683_*684insTT | |
| ENST00000231228.3:c.*201_*202insTT MANE Select | ENSP00000231228.2:n.*201_*202insTT | |
| ENST00000231228.2:c.*201_*202insTT | ENSP00000231228.2:n.*201_*202insTT | |
| NM_002187.2:c.*201_*202insTT , LRG_71t1:c.*201_*202insTT | NP_002178.2:n.*201_*202insTT | |
| NM_002187.3:c.*201_*202insTT MANE Select | NP_002178.2:n.*201_*202insTT |