Linked Data
MyVariant Identifiers:
chr17:g.42457024_42457118del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44379658_44379752del , CM000679.2:g.44379658_44379752del | GRCh38 |
| NC_000017.10:g.42457026_42457120del , CM000679.1:g.42457026_42457120del | GRCh37 |
| NC_000017.9:g.39812552_39812646del | NCBI36 |
| NG_008331.1:g.14756_14850del , LRG_479:g.14756_14850del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262407.6:c.1817_1878+33del | ||
| ENST00000648408.1:c.1248_1309+33del | ||
| ENST00000262407.5:c.1817_1878+33del | ||
| ENST00000592462.5:n.612_673+33del | ||
| NM_000419.3:c.1817_1878+33del , LRG_479t1:c.1817_1878+33del | ||
| XM_011524749.1:c.1817_1878+33del | ||
| XM_011524750.1:c.1817_1878+33del | ||
| NM_000419.4:c.1817_1878+33del | ||
| NM_000419.5:c.1817_1878+33del |