Linked Data
ClinVar Variation Id:
456163
dbSNP Id:
rs761347179
ExAC:
9:97934336 GATA / G
gnomAD v2:
9-97934336-GATA-G
gnomAD v3:
9-95172054-GATA-G
gnomAD v4:
9-95172054-GATA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95172055_95172057del , CM000671.2:g.95172055_95172057del | GRCh38 |
| NC_000009.11:g.97934337_97934339del , CM000671.1:g.97934337_97934339del | GRCh37 |
| NC_000009.10:g.96974158_96974160del | NCBI36 |
| NG_011707.1:g.150653_150655del , LRG_497:g.150653_150655del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696261.1:n.827_829del | ||
| ENST00000289081.8:c.436_438del MANE Select | ENSP00000289081.3:p.Tyr146del | |
| ENST00000375305.6:c.436_438del | ENSP00000364454.1:p.Tyr146del | |
| ENST00000490972.7:c.436_438del | ENSP00000479931.1:p.Tyr146del | |
| ENST00000636777.1:n.494_496del | ||
| ENST00000647778.1:c.436_438del | ENSP00000498125.1:p.Tyr146del | |
| ENST00000649334.1:c.581_583del | ENSP00000497735.1:n.581_583del | |
| ENST00000649701.1:n.151_153del | ||
| ENST00000289081.7:c.436_438del | ENSP00000289081.3:p.Tyr146del | |
| ENST00000375305.5:c.436_438del | ENSP00000364454.1:p.Tyr146del | |
| ENST00000433829.1:c.436_438del | ENSP00000406908.1:p.Tyr146del | |
| ENST00000474949.1:n.793_795del | ||
| ENST00000490972.6:c.436_438del | ENSP00000479931.1:p.Tyr146del | |
| NM_000136.2:c.436_438del , LRG_497t1:c.436_438del | NP_000127.2:p.Tyr146del | |
| NM_001243743.1:c.436_438del | NP_001230672.1:p.Tyr146del | |
| NM_001243744.1:c.436_438del | NP_001230673.1:p.Tyr146del | |
| XM_006717001.1:c.436_438del | XP_006717064.1:p.Tyr146del | |
| XM_006717002.2:c.436_438del | XP_006717065.1:p.Tyr146del | |
| XM_006717004.2:c.436_438del | XP_006717067.1:p.Tyr146del | |
| XM_011518365.1:c.436_438del | XP_011516667.1:p.Tyr146del | |
| XM_011518366.1:c.436_438del | XP_011516668.1:p.Tyr146del | |
| XM_011518367.1:c.-21_-19del | XP_011516669.1:n.-21_-19del | |
| XM_006717001.3:c.436_438del | XP_006717064.1:p.Tyr146del | |
| XM_006717002.4:c.436_438del | XP_006717065.1:p.Tyr146del | |
| XM_006717004.4:c.436_438del | XP_006717067.1:p.Tyr146del | |
| XM_011518365.3:c.436_438del | XP_011516667.1:p.Tyr146del | |
| XM_011518366.3:c.436_438del | XP_011516668.1:p.Tyr146del | |
| XM_011518367.2:c.-21_-19del | XP_011516669.1:n.-21_-19del | |
| XM_017014452.2:c.-21_-19del | XP_016869941.1:n.-21_-19del | |
| XM_017014453.1:c.-21_-19del | XP_016869942.1:n.-21_-19del | |
| XM_017014454.1:c.-21_-19del | XP_016869943.1:n.-21_-19del | |
| XM_024447451.1:c.436_438del | XP_024303219.1:p.Tyr146del | |
| NM_000136.3:c.436_438del MANE Select | NP_000127.2:p.Tyr146del | |
| NM_001243743.2:c.436_438del | NP_001230672.1:p.Tyr146del | |
| NM_001243744.2:c.436_438del | NP_001230673.1:p.Tyr146del |