Linked Data
dbSNP Id:
rs1467328300
MyVariant Identifiers:
chr6:g.32006161_32006162insTATA (hg19)
chr6:g.32038384_32038385insTATA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32038385_32038388dup , CM000668.2:g.32038385_32038388dup | GRCh38 |
| NC_000006.11:g.32006162_32006165dup , CM000668.1:g.32006162_32006165dup | GRCh37 |
| NC_000006.10:g.32114141_32114144dup | NCBI36 |
| NG_007941.2:g.5081_5084dup | |
| NG_007941.3:g.5081_5084dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000418967.6:c.-38_-35dup | ENSP00000408860.2:n.-38_-35dup | |
| ENST00000466779.5:c.-38_-35dup | ENSP00000417321.1:n.-38_-35dup | |
| ENST00000478281.5:c.-38_-35dup | ENSP00000419572.1:n.-38_-35dup | |
| ENST00000479074.5:n.21_24dup | ||
| ENST00000479730.5:n.21_24dup | ||
| ENST00000480027.1:n.16_19dup | ||
| ENST00000483041.5:n.16_19dup | ||
| ENST00000486063.5:n.46_49dup | ||
| NM_000500.7:c.-38_-35dup | NP_000491.4:n.-38_-35dup | |
| NM_001128590.3:c.-38_-35dup | NP_001122062.3:n.-38_-35dup | |
| XM_011514314.1:c.-462_-459dup | XP_011512616.1:n.-462_-459dup | |
| NM_001368143.1:c.-462_-459dup | NP_001355072.1:n.-462_-459dup | |
| NM_001368144.1:c.-372_-369dup | NP_001355073.1:n.-372_-369dup |