Canonical Allele Identifier:
CA155828858
Gene:
Linked Data
dbSNP Id:
rs958931463
gnomAD v3:
7-24283788-G-GGGTT
gnomAD v4:
7-24283788-G-GGGTT
MyVariant Identifiers:
chr7:g.24323407_24323408insGGTT (hg19)
chr7:g.24283788_24283789insGGTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24283792_24283795dup , CM000669.2:g.24283792_24283795dup | GRCh38 |
| NC_000007.13:g.24323411_24323414dup , CM000669.1:g.24323411_24323414dup | GRCh37 |
| NC_000007.12:g.24289936_24289939dup | NCBI36 |
| NG_016148.1:g.4605_4608dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017012910.1:c.42-28093_42-28090dup | XP_016868399.1:n.42-28093_42-28090dup | |
| XM_017012911.1:c.42-28093_42-28090dup | XP_016868400.1:n.42-28093_42-28090dup | |
| XR_001745121.1:n.473+35565_473+35568dup | ||
| XR_001745122.1:n.345-86763_345-86760dup | ||
| XR_001745123.1:n.473+35565_473+35568dup | ||
| XR_001745124.1:n.473+35565_473+35568dup | ||
| XR_001745125.1:n.473+35565_473+35568dup | ||
| XR_001745126.1:n.473+35565_473+35568dup | ||
| XR_001745127.1:n.345-28093_345-28090dup | ||
| XR_001745129.1:n.473+35565_473+35568dup | ||
| XR_001745130.1:n.473+35565_473+35568dup | ||
| XR_001745131.1:n.473+35565_473+35568dup | ||
| XR_001745132.1:n.473+35565_473+35568dup |