Linked Data
dbSNP Id:
rs34117656
MyVariant Identifiers:
chr10:g.103531444_103531445insG (hg19)
chr10:g.101771687_101771688insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.101771688dup , CM000672.2:g.101771688dup | GRCh38 |
| NC_000010.10:g.103531445dup , CM000672.1:g.103531445dup | GRCh37 |
| NC_000010.9:g.103521435dup | NCBI36 |
| NG_007151.1:g.9383dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320185.7:c.338-119dup MANE Select | ENSP00000321797.2:n.338-119dup | |
| ENST00000618991.5:c.26-119dup | ENSP00000484420.1:n.26-119dup | |
| ENST00000344255.8:c.305-119dup | ENSP00000340039.3:n.305-119dup | |
| ENST00000320185.6:c.338-119dup | ENSP00000321797.2:n.338-119dup | |
| ENST00000344255.7:c.305-119dup | ENSP00000340039.3:n.305-119dup | |
| ENST00000346714.7:c.218-119dup | ENSP00000344306.3:n.218-119dup | |
| ENST00000347978.2:c.251-119dup | ENSP00000321945.2:n.251-119dup | |
| ENST00000469792.6:c.*302-119dup | ENSP00000473299.1:n.*302-119dup | |
| ENST00000485728.1:n.214-119dup | ||
| ENST00000618991.4:c.26-119dup | ENSP00000484420.1:n.26-119dup | |
| NM_001206389.1:c.26-119dup | NP_001193318.1:n.26-119dup | |
| NM_006119.4:c.251-119dup | NP_006110.1:n.251-119dup | |
| NM_033163.3:c.338-119dup | NP_149353.1:n.338-119dup | |
| NM_033164.3:c.305-119dup | NP_149354.1:n.305-119dup | |
| NM_033165.3:c.218-119dup | NP_149355.1:n.218-119dup | |
| XM_011539509.1:c.260-119dup | XP_011537811.1:n.260-119dup | |
| XR_946252.2:n.490dup | ||
| XR_946253.2:n.488dup | ||
| NM_006119.5:c.251-119dup | NP_006110.1:n.251-119dup | |
| NM_033163.4:c.338-119dup | NP_149353.1:n.338-119dup | |
| NM_033164.4:c.305-119dup | NP_149354.1:n.305-119dup | |
| NM_033165.4:c.218-119dup | NP_149355.1:n.218-119dup | |
| NM_001206389.2:c.26-119dup | NP_001193318.1:n.26-119dup | |
| NM_006119.6:c.251-119dup | NP_006110.1:n.251-119dup | |
| NM_033163.5:c.338-119dup MANE Select | NP_149353.1:n.338-119dup | |
| NM_033165.5:c.218-119dup | NP_149355.1:n.218-119dup |