Linked Data
dbSNP Id:
rs1064795929
MyVariant Identifiers:
chr9:g.98011664_98011665insAACA (hg19)
chr9:g.95249382_95249383insAACA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95249385_95249388dup , CM000671.2:g.95249385_95249388dup | GRCh38 |
| NC_000009.11:g.98011667_98011670dup , CM000671.1:g.98011667_98011670dup | GRCh37 |
| NC_000009.10:g.97051488_97051491dup | NCBI36 |
| NG_011707.1:g.73324_73327dup , LRG_497:g.73324_73327dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696261.1:n.169-17_169-14dup | ||
| ENST00000696262.1:c.-78-17_-78-14dup | ENSP00000512510.1:n.-78-17_-78-14dup | |
| ENST00000696263.1:n.178-17_178-14dup | ||
| ENST00000289081.8:c.-78-17_-78-14dup MANE Select | ENSP00000289081.3:n.-78-17_-78-14dup | |
| ENST00000375305.6:c.-78-17_-78-14dup | ENSP00000364454.1:n.-78-17_-78-14dup | |
| ENST00000490972.7:c.-78-17_-78-14dup | ENSP00000479931.1:n.-78-17_-78-14dup | |
| ENST00000636777.1:n.20-56_20-53dup | ||
| ENST00000647778.1:c.-78-17_-78-14dup | ENSP00000498125.1:n.-78-17_-78-14dup | |
| ENST00000647882.1:c.-78-17_-78-14dup | ENSP00000497025.1:n.-78-17_-78-14dup | |
| ENST00000648415.1:n.1561-17_1561-14dup | ||
| ENST00000649519.1:c.-78-17_-78-14dup | ENSP00000497630.1:n.-78-17_-78-14dup | |
| ENST00000649611.1:c.-78-17_-78-14dup | ENSP00000497986.1:n.-78-17_-78-14dup | |
| ENST00000650176.1:n.103-17_103-14dup | ||
| ENST00000289081.7:c.-78-17_-78-14dup | ENSP00000289081.3:n.-78-17_-78-14dup | |
| ENST00000375305.5:c.-78-17_-78-14dup | ENSP00000364454.1:n.-78-17_-78-14dup | |
| ENST00000433829.1:c.-78-17_-78-14dup | ENSP00000406908.1:n.-78-17_-78-14dup | |
| ENST00000474949.1:n.185-17_185-14dup | ||
| ENST00000490972.6:c.-78-17_-78-14dup | ENSP00000479931.1:n.-78-17_-78-14dup | |
| NM_000136.2:c.-78-17_-78-14dup , LRG_497t1:c.-78-17_-78-14dup | NP_000127.2:n.-78-17_-78-14dup | |
| NM_001243743.1:c.-78-17_-78-14dup | NP_001230672.1:n.-78-17_-78-14dup | |
| NM_001243744.1:c.-78-17_-78-14dup | NP_001230673.1:n.-78-17_-78-14dup | |
| XM_006717001.1:c.-78-17_-78-14dup | XP_006717064.1:n.-78-17_-78-14dup | |
| XM_006717002.2:c.-78-17_-78-14dup | XP_006717065.1:n.-78-17_-78-14dup | |
| XM_006717004.2:c.-78-17_-78-14dup | XP_006717067.1:n.-78-17_-78-14dup | |
| XM_011518365.1:c.-78-17_-78-14dup | XP_011516667.1:n.-78-17_-78-14dup | |
| XM_011518366.1:c.-78-17_-78-14dup | XP_011516668.1:n.-78-17_-78-14dup | |
| XM_011518367.1:c.-679-17_-679-14dup | XP_011516669.1:n.-679-17_-679-14dup | |
| XM_006717001.3:c.-78-17_-78-14dup | XP_006717064.1:n.-78-17_-78-14dup | |
| XM_006717002.4:c.-78-17_-78-14dup | XP_006717065.1:n.-78-17_-78-14dup | |
| XM_006717004.4:c.-78-17_-78-14dup | XP_006717067.1:n.-78-17_-78-14dup | |
| XM_011518365.3:c.-78-17_-78-14dup | XP_011516667.1:n.-78-17_-78-14dup | |
| XM_011518366.3:c.-78-17_-78-14dup | XP_011516668.1:n.-78-17_-78-14dup | |
| XM_011518367.2:c.-679-17_-679-14dup | XP_011516669.1:n.-679-17_-679-14dup | |
| XM_017014452.2:c.-679-17_-679-14dup | XP_016869941.1:n.-679-17_-679-14dup | |
| XM_017014453.1:c.-679-17_-679-14dup | XP_016869942.1:n.-679-17_-679-14dup | |
| XM_017014454.1:c.-679-17_-679-14dup | XP_016869943.1:n.-679-17_-679-14dup | |
| XM_024447451.1:c.-78-17_-78-14dup | XP_024303219.1:n.-78-17_-78-14dup | |
| NM_000136.3:c.-78-17_-78-14dup MANE Select | NP_000127.2:n.-78-17_-78-14dup | |
| NM_001243743.2:c.-78-17_-78-14dup | NP_001230672.1:n.-78-17_-78-14dup | |
| NM_001243744.2:c.-78-17_-78-14dup | NP_001230673.1:n.-78-17_-78-14dup |