Linked Data
dbSNP Id:
rs2065072510
gnomAD v2:
10-103534921-CG-C
gnomAD v4:
10-101775164-CG-C
MyVariant Identifiers:
chr10:g.103534922del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.101775166del , CM000672.2:g.101775166del | GRCh38 |
| NC_000010.10:g.103534923del , CM000672.1:g.103534923del | GRCh37 |
| NC_000010.9:g.103524913del | NCBI36 |
| NG_007151.1:g.5906del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320185.7:c.121del MANE Select | ENSP00000321797.2:p.Arg41GlyfsTer13 | |
| ENST00000618991.5:c.-123-286del | ENSP00000484420.1:n.-123-286del | |
| ENST00000344255.8:c.121del | ENSP00000340039.3:p.Arg41GlyfsTer14 | |
| ENST00000320185.6:c.121del | ENSP00000321797.2:p.Arg41GlyfsTer13 | |
| ENST00000344255.7:c.121del | ENSP00000340039.3:p.Arg41GlyfsTer14 | |
| ENST00000346714.7:c.70-286del | ENSP00000344306.3:n.70-286del | |
| ENST00000347978.2:c.70-253del | ENSP00000321945.2:n.70-253del | |
| ENST00000469792.6:c.*154-286del | ENSP00000473299.1:n.*154-286del | |
| ENST00000485728.1:n.33-253del | ||
| ENST00000618991.4:c.-123-286del | ENSP00000484420.1:n.-123-286del | |
| NM_001206389.1:c.-123-286del | NP_001193318.1:n.-123-286del | |
| NM_006119.4:c.70-253del | NP_006110.1:n.70-253del | |
| NM_033163.3:c.121del | NP_149353.1:p.Arg41GlyfsTer13 | |
| NM_033164.3:c.121del | NP_149354.1:p.Arg41GlyfsTer14 | |
| NM_033165.3:c.70-286del | NP_149355.1:n.70-286del | |
| XM_011539509.1:c.79-253del | XP_011537811.1:n.79-253del | |
| NM_006119.5:c.70-253del | NP_006110.1:n.70-253del | |
| NM_033163.4:c.121del | NP_149353.1:p.Arg41GlyfsTer13 | |
| NM_033164.4:c.121del | NP_149354.1:p.Arg41GlyfsTer14 | |
| NM_033165.4:c.70-286del | NP_149355.1:n.70-286del | |
| NM_001206389.2:c.-123-286del | NP_001193318.1:n.-123-286del | |
| NM_006119.6:c.70-253del | NP_006110.1:n.70-253del | |
| NM_033163.5:c.121del MANE Select | NP_149353.1:p.Arg41GlyfsTer13 | |
| NM_033165.5:c.70-286del | NP_149355.1:n.70-286del |