Canonical Allele Identifier:
CA803778365
Gene:
Linked Data
dbSNP Id:
rs1394911889
MyVariant Identifiers:
chr5:g.128722525_128722526insCTC (hg19)
chr5:g.129386832_129386833insCTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.129386833_129386835dup , CM000667.2:g.129386833_129386835dup | GRCh38 |
| NC_000005.9:g.128722526_128722528dup , CM000667.1:g.128722526_128722528dup | GRCh37 |
| NC_000005.8:g.128750425_128750427dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_427770.2:n.163-1615_163-1613dup | ||
| XR_948774.1:n.235-5818_235-5816dup | ||
| XR_001742463.1:n.4089-1615_4089-1613dup | ||
| XR_001742464.1:n.2019-5818_2019-5816dup | ||
| XR_001742465.1:n.401-1615_401-1613dup | ||
| XR_427770.3:n.337-1615_337-1613dup |