Linked Data
dbSNP Id:
rs1230417376
gnomAD v3:
9-72577887-T-TTTAC
gnomAD v4:
9-72577887-T-TTTAC
MyVariant Identifiers:
chr9:g.75192803_75192804insTTAC (hg19)
chr9:g.72577887_72577888insTTAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.72577890_72577891insCTTA , CM000671.2:g.72577890_72577891insCTTA | GRCh38 |
| NC_000009.11:g.75192806_75192807insCTTA , CM000671.1:g.75192806_75192807insCTTA | GRCh37 |
| NC_000009.10:g.74382626_74382627insCTTA | NCBI36 |
| NG_008213.1:g.61090_61091insCTTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297784.10:c.-427-12_-427-11insCTTA MANE Select | ENSP00000297784.6:n.-427-12_-427-11insCTTA | |
| ENST00000643676.1:n.307-38478_307-38477insCTTA | ||
| ENST00000645208.2:c.-439_-438insCTTA | ENSP00000494684.1:n.-439_-438insCTTA | |
| ENST00000650689.1:n.66-12_66-11insCTTA | ||
| ENST00000651183.1:c.-528-12_-528-11insCTTA | ENSP00000498723.1:n.-528-12_-528-11insCTTA | |
| ENST00000651743.1:n.116-12_116-11insCTTA | ||
| ENST00000297784.9:c.-427-12_-427-11insCTTA | ENSP00000297784.5:n.-427-12_-427-11insCTTA | |
| ENST00000497073.1:n.103_104insCTTA | ||
| NM_138691.2:c.-427-12_-427-11insCTTA | NP_619636.2:n.-427-12_-427-11insCTTA | |
| NM_138691.3:c.-427-12_-427-11insCTTA MANE Select | NP_619636.2:n.-427-12_-427-11insCTTA |