Linked Data
ClinVar Variation Id:
199100
dbSNP Id:
rs796065336
MyVariant Identifiers:
chr1:g.10689923_10689924delinsGT (hg19)
chr1:g.10629866_10629867delinsGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.10629866_10629867delinsGT , CM000663.2:g.10629866_10629867delinsGT | GRCh38 |
| NC_000001.10:g.10689923_10689924delinsGT , CM000663.1:g.10689923_10689924delinsGT | GRCh37 |
| NC_000001.9:g.10612510_10612511delinsGT | NCBI36 |
| NG_008340.1:g.159921_159922delinsGT | |
| NG_008340.2:g.159921_159922delinsGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356607.9:c.1013_1014delinsGT MANE Select | ENSP00000349016.4:p.Asp338Gly | |
| ENST00000356607.8:c.1013_1014delinsGT | ENSP00000349016.4:p.Asp338Gly | |
| NM_004565.2:c.1013_1014delinsGT | NP_004556.1:p.Asp338Gly | |
| XM_005263470.3:c.821_822delinsGT | XP_005263527.1:p.Asp274Gly | |
| XM_011541577.1:c.1055_1056delinsGT | XP_011539879.1:p.Asp352Gly | |
| XM_011541578.1:c.956_957delinsGT | XP_011539880.1:p.Asp319Gly | |
| XM_011541579.1:c.926_927delinsGT | XP_011539881.1:p.Asp309Gly | |
| XM_011541580.1:c.884_885delinsGT | XP_011539882.1:p.Asp295Gly | |
| XM_005263470.5:c.821_822delinsGT | XP_005263527.1:p.Asp274Gly | |
| XM_011541577.2:c.1055_1056delinsGT | XP_011539879.1:p.Asp352Gly | |
| XM_011541578.2:c.956_957delinsGT | XP_011539880.1:p.Asp319Gly | |
| XM_011541579.3:c.926_927delinsGT | XP_011539881.1:p.Asp309Gly | |
| XM_024447651.1:c.821_822delinsGT | XP_024303419.1:p.Asp274Gly | |
| NM_004565.3:c.1013_1014delinsGT MANE Select | NP_004556.1:p.Asp338Gly |