Linked Data
ClinVar Variation Id:
208717
dbSNP Id:
rs797044907
gnomAD v3:
11-72108662-C-CAGCT
gnomAD v4:
11-72108662-C-CAGCT
MyVariant Identifiers:
chr11:g.71819708_71819709insAGCT (hg19)
chr11:g.72108662_72108663insAGCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72108663_72108666dup , CM000673.2:g.72108663_72108666dup | GRCh38 |
| NC_000011.9:g.71819709_71819712dup , CM000673.1:g.71819709_71819712dup | GRCh37 |
| NC_000011.8:g.71497357_71497360dup | NCBI36 |
| NG_021423.1:g.33328_33331dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000541899.3:c.515_518dup (TOMT) MANE Select | ENSP00000494667.1:p.Ser174AlafsTer? | |
| ENST00000541899.2:c.515_518dup (TOMT) | ENSP00000494667.1:p.Ser174AlafsTer? | |
| ENST00000643715.1:c.*25_*28dup (LRTOMT) | ENSP00000496019.1:n.*25_*28dup | |
| ENST00000307198.11:c.614_617dup (LRRC51) | ENSP00000305742.7:p.Ser207AlafsTer? | |
| ENST00000419228.2:c.*25_*28dup (LRRC51) | ENSP00000392233.2:n.*25_*28dup | |
| ENST00000427369.6:c.*333_*336dup (LRRC51) | ENSP00000409403.2:n.*333_*336dup | |
| ENST00000435085.5:c.614_617dup (LRRC51) | ENSP00000409789.1:p.Ser207AlafsTer? | |
| ENST00000439209.5:c.*25_*28dup (LRRC51) | ENSP00000395139.1:n.*25_*28dup | |
| ENST00000502597.2:c.64-1061_64-1058dup (ANAPC15) | ENSP00000441774.1:n.64-1061_64-1058dup | |
| ENST00000543050.5:c.319-1061_319-1058dup (ANAPC15) | ENSP00000437360.1:n.319-1061_319-1058dup | |
| ENST00000544409.5:c.*333_*336dup (LRRC51) | ENSP00000440969.1:n.*333_*336dup | |
| NM_001145308.4:c.614_617dup (LRTOMT) | NP_001138780.1:p.Ser207AlafsTer? | |
| NM_001145309.3:c.614_617dup (LRTOMT) | NP_001138781.1:p.Ser207AlafsTer? | |
| NM_001145310.3:c.494_497dup (LRTOMT) | NP_001138782.1:p.Ser167AlafsTer? | |
| XM_011544849.1:c.839_842dup (LRTOMT) | XP_011543151.1:p.Ser282AlafsTer? | |
| NM_001330321.1:c.319-1061_319-1058dup (ANAPC15) | NP_001317250.1:n.319-1061_319-1058dup | |
| XM_024448401.1:c.839_842dup (LRTOMT) | XP_024304169.1:p.Ser282AlafsTer? | |
| NM_001145308.5:c.614_617dup (LRTOMT) | NP_001138780.1:p.Ser207AlafsTer? | |
| NM_001145309.4:c.614_617dup (LRTOMT) | NP_001138781.1:p.Ser207AlafsTer? | |
| NM_001145310.4:c.494_497dup (LRTOMT) | NP_001138782.1:p.Ser167AlafsTer? | |
| NM_001330321.2:c.319-1061_319-1058dup (ANAPC15) | NP_001317250.1:n.319-1061_319-1058dup | |
| NM_001393427.1:c.319-1061_319-1058dup (ANAPC15) | NP_001380356.1:n.319-1061_319-1058dup | |
| NM_001393428.1:c.319-1061_319-1058dup (ANAPC15) | NP_001380357.1:n.319-1061_319-1058dup | |
| NM_001393429.1:c.319-1061_319-1058dup (ANAPC15) | NP_001380358.1:n.319-1061_319-1058dup | |
| NM_001393430.1:c.319-1061_319-1058dup (ANAPC15) | NP_001380359.1:n.319-1061_319-1058dup | |
| NM_001393431.1:c.319-1061_319-1058dup (ANAPC15) | NP_001380360.1:n.319-1061_319-1058dup | |
| NM_001393443.1:c.*153_*156dup (ANAPC15) | NP_001380372.1:n.*153_*156dup | |
| NM_001393444.1:c.*153_*156dup (ANAPC15) | NP_001380373.1:n.*153_*156dup | |
| NM_001393445.1:c.*153_*156dup (ANAPC15) | NP_001380374.1:n.*153_*156dup | |
| NM_001393459.1:c.64-1061_64-1058dup (ANAPC15) | NP_001380388.1:n.64-1061_64-1058dup | |
| NM_001393500.1:c.515_518dup (TOMT) | NP_001380429.1:p.Ser174AlafsTer? | |
| NR_171687.1:n.777_780dup (ANAPC15) | ||
| NM_001393500.2:c.515_518dup (TOMT) MANE Select | NP_001380429.1:p.Ser174AlafsTer? |