Linked Data
dbSNP Id:
rs1568677153
gnomAD v2:
17-36104917-G-GGT
gnomAD v4:
17-37744926-G-GGT
MyVariant Identifiers:
chr17:g.36104917_36104918insGT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.37744926_37744927insGT , CM000679.2:g.37744926_37744927insGT | GRCh38 |
| NC_000017.10:g.36104917_36104918insGT , CM000679.1:g.36104917_36104918insGT | GRCh37 |
| NC_000017.9:g.33179030_33179031insGT | NCBI36 |
| NG_013019.2:g.5180_5181insAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617811.5:c.-43_-42insAC MANE Select | ENSP00000480291.1:n.-43_-42insAC | |
| ENST00000613727.4:c.-43_-42insAC | ENSP00000477524.1:n.-43_-42insAC | |
| ENST00000614313.4:c.-43_-42insAC | ENSP00000482529.1:n.-43_-42insAC | |
| ENST00000617272.4:c.-43_-42insAC | ENSP00000478682.1:n.-43_-42insAC | |
| ENST00000617811.4:c.-43_-42insAC | ENSP00000480291.1:n.-43_-42insAC | |
| ENST00000620125.1:c.-43_-42insAC | ENSP00000481245.1:n.-43_-42insAC | |
| ENST00000621123.4:c.-43_-42insAC | ENSP00000482711.1:n.-43_-42insAC | |
| NM_000458.3:c.-43_-42insAC | NP_000449.1:n.-43_-42insAC | |
| NM_001165923.3:c.-43_-42insAC | NP_001159395.1:n.-43_-42insAC | |
| NM_001304286.1:c.-43_-42insAC | NP_001291215.1:n.-43_-42insAC | |
| XM_011525160.1:c.-43_-42insAC | XP_011523462.1:n.-43_-42insAC | |
| XM_011525161.1:c.-43_-42insAC | XP_011523463.1:n.-43_-42insAC | |
| XM_011525162.1:c.-43_-42insAC | XP_011523464.1:n.-43_-42insAC | |
| XM_011525163.1:c.-43_-42insAC | XP_011523465.1:n.-43_-42insAC | |
| XM_011525164.1:c.-43_-42insAC | XP_011523466.1:n.-43_-42insAC | |
| XM_011525162.2:c.-43_-42insAC | XP_011523464.1:n.-43_-42insAC | |
| XM_011525163.2:c.-43_-42insAC | XP_011523465.1:n.-43_-42insAC | |
| NM_000458.4:c.-43_-42insAC MANE Select | NP_000449.1:n.-43_-42insAC | |
| NM_001165923.4:c.-43_-42insAC | NP_001159395.1:n.-43_-42insAC | |
| NM_001304286.2:c.-43_-42insAC | NP_001291215.1:n.-43_-42insAC |