Linked Data
gnomAD v2:
17-42429374-A-AC
gnomAD v4:
17-44352006-A-AC
MyVariant Identifiers:
chr17:g.42429375_42429376insC (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44352012dup , CM000679.2:g.44352012dup | GRCh38 |
| NC_000017.10:g.42429380dup , CM000679.1:g.42429380dup | GRCh37 |
| NC_000017.9:g.39784906dup | NCBI36 |
| NG_007886.1:g.11890dup , LRG_661:g.11890dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000053867.8:c.1180-3dup MANE Select | ENSP00000053867.2:n.1180-3dup | |
| ENST00000639447.1:c.1136+260dup | ENSP00000492014.1:n.1136+260dup | |
| ENST00000053867.7:c.1180-3dup | ENSP00000053867.2:n.1180-3dup | |
| ENST00000586443.1:c.621-3dup | ||
| ENST00000589265.5:c.709-3dup | ENSP00000467616.1:n.709-3dup | |
| NM_002087.3:c.1180-3dup | NP_002078.1:n.1180-3dup | |
| XM_005257253.1:c.1180-3dup | XP_005257310.1:n.1180-3dup | |
| XM_024450730.1:c.1180-3dup | XP_024306498.1:n.1180-3dup | |
| NM_002087.4:c.1180-3dup MANE Select | NP_002078.1:n.1180-3dup |