Linked Data
dbSNP Id:
rs1554477762
gnomAD v3:
8-1857883-T-TATCTATCG
gnomAD v4:
8-1857883-T-TATCTATCG
MyVariant Identifiers:
chr8:g.1806049_1806050insATCTATCG (hg19)
chr8:g.1857883_1857884insATCTATCG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.1857890_1857891insGATCTATC , CM000670.2:g.1857890_1857891insGATCTATC | GRCh38 |
| NC_000008.10:g.1806056_1806057insGATCTATC , CM000670.1:g.1806056_1806057insGATCTATC | GRCh37 |
| NC_000008.9:g.1793463_1793464insGATCTATC | NCBI36 |
| NG_008480.1:g.38908_38909insGATCTATC , LRG_234:g.38908_38909insGATCTATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349830.8:c.38-70_38-69insGATCTATC MANE Select | ENSP00000340297.3:n.38-70_38-69insGATCTATC | |
| ENST00000635773.1:c.497-70_497-69insGATCTATC | ||
| ENST00000635855.1:c.628-70_628-69insGATCTATC | ENSP00000489726.1:n.628-70_628-69insGATCTATC | |
| ENST00000636175.1:c.428-70_428-69insGATCTATC | ||
| ENST00000349830.7:c.38-70_38-69insGATCTATC | ENSP00000340297.3:n.38-70_38-69insGATCTATC | |
| ENST00000398564.5:c.110-70_110-69insGATCTATC | ENSP00000381571.1:n.110-70_110-69insGATCTATC | |
| ENST00000518288.5:c.110-70_110-69insGATCTATC | ENSP00000431012.1:n.110-70_110-69insGATCTATC | |
| ENST00000520359.5:c.38-70_38-69insGATCTATC | ENSP00000427909.1:n.38-70_38-69insGATCTATC | |
| NM_001308152.1:c.38-70_38-69insGATCTATC | NP_001295081.1:n.38-70_38-69insGATCTATC | |
| NM_001308153.1:c.110-70_110-69insGATCTATC | NP_001295082.1:n.110-70_110-69insGATCTATC | |
| NM_014629.2:c.38-70_38-69insGATCTATC , LRG_234t1:c.38-70_38-69insGATCTATC | NP_055444.2:n.38-70_38-69insGATCTATC | |
| NM_014629.3:c.38-70_38-69insGATCTATC | NP_055444.2:n.38-70_38-69insGATCTATC | |
| XM_005266041.2:c.38-70_38-69insGATCTATC | XP_005266098.1:n.38-70_38-69insGATCTATC | |
| XM_011534766.1:c.38-70_38-69insGATCTATC | XP_011533068.1:n.38-70_38-69insGATCTATC | |
| XM_011534767.1:c.38-70_38-69insGATCTATC | XP_011533069.1:n.38-70_38-69insGATCTATC | |
| XM_011534768.1:c.38-70_38-69insGATCTATC | XP_011533070.1:n.38-70_38-69insGATCTATC | |
| XM_011534769.1:c.-8-70_-8-69insGATCTATC | XP_011533071.1:n.-8-70_-8-69insGATCTATC | |
| XM_011534770.1:c.38-70_38-69insGATCTATC | XP_011533072.1:n.38-70_38-69insGATCTATC | |
| XM_005266041.4:c.38-70_38-69insGATCTATC | XP_005266098.1:n.38-70_38-69insGATCTATC | |
| XM_011534767.2:c.38-70_38-69insGATCTATC | XP_011533069.1:n.38-70_38-69insGATCTATC | |
| XM_011534770.2:c.38-70_38-69insGATCTATC | XP_011533072.1:n.38-70_38-69insGATCTATC | |
| XM_017014003.1:c.110-70_110-69insGATCTATC | XP_016869492.1:n.110-70_110-69insGATCTATC | |
| XM_024447334.1:c.38-70_38-69insGATCTATC | XP_024303102.1:n.38-70_38-69insGATCTATC | |
| XM_024447335.1:c.122-70_122-69insGATCTATC | XP_024303103.1:n.122-70_122-69insGATCTATC | |
| NM_014629.4:c.38-70_38-69insGATCTATC MANE Select | NP_055444.2:n.38-70_38-69insGATCTATC | |
| NM_001308152.2:c.38-70_38-69insGATCTATC | NP_001295081.1:n.38-70_38-69insGATCTATC | |
| NM_001308153.2:c.110-70_110-69insGATCTATC | NP_001295082.1:n.110-70_110-69insGATCTATC |