Linked Data
dbSNP Id:
rs1445015551
MyVariant Identifiers:
chr5:g.1444588_1444589insGTTGTGTGT (hg19)
chr5:g.1444473_1444474insGTTGTGTGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1444473_1444474insGTTGTGTGT , CM000667.2:g.1444473_1444474insGTTGTGTGT | GRCh38 |
| NC_000005.9:g.1444588_1444589insGTTGTGTGT , CM000667.1:g.1444588_1444589insGTTGTGTGT | GRCh37 |
| NC_000005.8:g.1497588_1497589insGTTGTGTGT | NCBI36 |
| NG_015885.1:g.5955_5956insACACACAAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.-46+874_-46+875insACACACAAC MANE Select | ENSP00000270349.9:n.-46+874_-46+875insACACACAAC | |
| ENST00000270349.11:c.-46+874_-46+875insACACACAAC | ENSP00000270349.9:n.-46+874_-46+875insACACACAAC | |
| NM_001044.4:c.-46+874_-46+875insACACACAAC | NP_001035.1:n.-46+874_-46+875insACACACAAC | |
| NM_001044.5:c.-46+874_-46+875insACACACAAC MANE Select | NP_001035.1:n.-46+874_-46+875insACACACAAC |