Canonical Allele Identifier:
CA10587407
Gene:
Linked Data
dbSNP Id:
rs886038300
MyVariant Identifiers:
chrY:g.555387_555397dupCCCGCGCGCCC (hg19)
chrY:g.644652_644662dupCCCGCGCGCCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.644652_644662dup , CM000686.2:g.644652_644662dup | GRCh38 |
| NC_000024.9:g.555387_555397dup , CM000686.1:g.555387_555397dup | GRCh37 |
| NC_000024.8:g.525387_525397dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711141.1:c.633+3565_633+3575dup | ENSP00000518639.1:n.633+3565_633+3575dup | |
| ENST00000711142.1:c.*16_*26dup | ENSP00000518640.1:n.*16_*26dup | |
| ENST00000711143.1:c.633+3565_633+3575dup | ENSP00000518641.1:n.633+3565_633+3575dup | |
| ENST00000711145.1:c.*16_*26dup | ENSP00000518642.1:n.*16_*26dup |