Linked Data
MyVariant Identifiers:
chr1:g.215901703dup (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728361dup , CM000663.2:g.215728361dup | GRCh38 |
| NC_000001.10:g.215901703dup , CM000663.1:g.215901703dup | GRCh37 |
| NC_000001.9:g.213968326dup | NCBI36 |
| NG_009497.1:g.700036dup | |
| NG_009497.2:g.700088dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11735dup MANE Select | ENSP00000305941.3:p.Ser3913ValfsTer12 | |
| ENST00000674083.1:c.11735dup | ENSP00000501296.1:p.Ser3913ValfsTer12 | |
| ENST00000307340.7:c.11735dup | ENSP00000305941.3:p.Ser3913ValfsTer12 | |
| NM_206933.2:c.11735dup | NP_996816.2:p.Ser3913ValfsTer12 | |
| NM_206933.3:c.11735dup | NP_996816.2:p.Ser3913ValfsTer12 | |
| NM_206933.4:c.11735dup MANE Select | NP_996816.3:p.Ser3913ValfsTer12 |