Linked Data
dbSNP Id:
rs1555204811
gnomAD v2:
11-118955914-TCCGAG-T
gnomAD v3:
11-119085204-TCCGAG-T
gnomAD v4:
11-119085204-TCCGAG-T
MyVariant Identifiers:
chr11:g.118955915_118955923delinsTAGC (hg19)
chr11:g.119085205_119085213delinsTAGC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119085205_119085209del , CM000673.2:g.119085205_119085209del | GRCh38 |
| NC_000011.9:g.118955915_118955919del , CM000673.1:g.118955915_118955919del | GRCh37 |
| NC_000011.8:g.118461125_118461129del | NCBI36 |
| NG_008093.1:g.5329_5333del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442944.7:c.33+139_33+143del | ENSP00000392041.3:n.33+139_33+143del | |
| ENST00000534956.2:n.36+139_36+143del | ||
| ENST00000536813.6:c.-102+139_-102+143del | ENSP00000438726.2:n.-102+139_-102+143del | |
| ENST00000546302.6:c.33+139_33+143del | ENSP00000445599.1:n.33+139_33+143del | |
| ENST00000640813.1:c.-19+139_-19+143del | ENSP00000491061.1:n.-19+139_-19+143del | |
| ENST00000648026.1:c.27+139_27+143del | ENSP00000498044.1:n.27+139_27+143del | |
| ENST00000649868.1:c.33+139_33+143del | ENSP00000497548.1:n.33+139_33+143del | |
| ENST00000652429.1:c.33+139_33+143del MANE Select | ENSP00000498786.1:n.33+139_33+143del | |
| ENST00000278715.7:c.33+139_33+143del | ENSP00000278715.3:n.33+139_33+143del | |
| ENST00000442944.6:c.-102+139_-102+143del | ENSP00000392041.2:n.-102+139_-102+143del | |
| ENST00000535793.5:c.33+139_33+143del | ENSP00000439904.1:n.33+139_33+143del | |
| ENST00000536185.5:n.201+139_201+143del | ||
| ENST00000536813.5:c.33+139_33+143del | ENSP00000438726.1:n.33+139_33+143del | |
| ENST00000537841.5:c.-19+48_-19+52del | ENSP00000444730.1:n.-19+48_-19+52del | |
| ENST00000542044.5:n.158+139_158+143del | ||
| ENST00000542729.5:c.-19+48_-19+52del | ENSP00000443058.1:n.-19+48_-19+52del | |
| ENST00000542822.5:c.124+48_124+52del | ENSP00000444817.1:n.124+48_124+52del | |
| ENST00000543090.5:c.33+139_33+143del | ENSP00000445429.1:n.33+139_33+143del | |
| ENST00000543821.5:n.179+139_179+143del | ||
| ENST00000544387.5:c.33+139_33+143del | ENSP00000438424.1:n.33+139_33+143del | |
| ENST00000545621.5:c.33+139_33+143del | ENSP00000444849.1:n.33+139_33+143del | |
| ENST00000545901.5:n.186+139_186+143del | ||
| ENST00000546302.5:c.33+139_33+143del | ENSP00000445599.1:n.33+139_33+143del | |
| NM_000190.3:c.33+139_33+143del | NP_000181.2:n.33+139_33+143del | |
| NM_001258208.1:c.33+139_33+143del | NP_001245137.1:n.33+139_33+143del | |
| NM_001258209.1:c.-19+48_-19+52del | NP_001245138.1:n.-19+48_-19+52del | |
| XM_005271531.1:c.-19+48_-19+52del | XP_005271588.1:n.-19+48_-19+52del | |
| XM_005271532.1:c.-19+72_-19+76del | XP_005271589.1:n.-19+72_-19+76del | |
| XM_005271533.2:c.33+139_33+143del | XP_005271590.1:n.33+139_33+143del | |
| NM_000190.4:c.33+139_33+143del MANE Select | NP_000181.2:n.33+139_33+143del | |
| XM_005271533.3:c.33+139_33+143del | XP_005271590.1:n.33+139_33+143del | |
| XM_024448460.1:c.33+139_33+143del | XP_024304228.1:n.33+139_33+143del | |
| NM_001258208.2:c.33+139_33+143del | NP_001245137.1:n.33+139_33+143del | |
| NM_001258209.2:c.-19+48_-19+52del | NP_001245138.1:n.-19+48_-19+52del |