Linked Data
dbSNP Id:
rs1231015609
gnomAD v2:
17-19552441-C-CTATG
MyVariant Identifiers:
chr17:g.19552441_19552442insTATG (hg19)
chr17:g.19649128_19649129insTATG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.19649128_19649129insTATG , CM000679.2:g.19649128_19649129insTATG | GRCh38 |
| NC_000017.10:g.19552441_19552442insTATG , CM000679.1:g.19552441_19552442insTATG | GRCh37 |
| NC_000017.9:g.19493033_19493034insTATG | NCBI36 |
| NG_007095.2:g.5378_5379insTATG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000176643.11:c.153+4_153+5insTATG MANE Select | ENSP00000176643.6:n.153+4_153+5insTATG | |
| ENST00000395575.7:c.153+4_153+5insTATG | ENSP00000378942.3:n.153+4_153+5insTATG | |
| ENST00000446398.7:n.163+4_163+5insTATG | ||
| ENST00000467473.6:n.276+4_276+5insTATG | ||
| ENST00000472059.6:c.153+4_153+5insTATG | ENSP00000458397.1:n.153+4_153+5insTATG | |
| ENST00000581518.6:c.153+4_153+5insTATG | ENSP00000461916.2:n.153+4_153+5insTATG | |
| ENST00000582991.6:c.153+4_153+5insTATG | ENSP00000464153.1:n.153+4_153+5insTATG | |
| ENST00000671878.1:c.153+4_153+5insTATG | ENSP00000500516.1:n.153+4_153+5insTATG | |
| ENST00000672357.1:c.153+4_153+5insTATG | ENSP00000500092.1:n.153+4_153+5insTATG | |
| ENST00000672465.1:c.153+4_153+5insTATG | ENSP00000500517.1:n.153+4_153+5insTATG | |
| ENST00000672487.1:c.153+4_153+5insTATG | ENSP00000500740.1:n.153+4_153+5insTATG | |
| ENST00000672564.1:n.374+4_374+5insTATG | ||
| ENST00000672567.1:c.44+4_44+5insTATG | ||
| ENST00000672709.1:c.7+4_7+5insTATG | ||
| ENST00000673136.1:c.153+4_153+5insTATG | ENSP00000500380.1:n.153+4_153+5insTATG | |
| ENST00000176643.10:c.153+4_153+5insTATG | ENSP00000176643.6:n.153+4_153+5insTATG | |
| ENST00000339618.8:c.153+4_153+5insTATG | ENSP00000345774.4:n.153+4_153+5insTATG | |
| ENST00000395575.6:c.153+4_153+5insTATG | ENSP00000378942.2:n.153+4_153+5insTATG | |
| ENST00000446398.6:c.153+4_153+5insTATG | ENSP00000395845.2:n.153+4_153+5insTATG | |
| ENST00000467473.5:n.310+4_310+5insTATG | ||
| ENST00000472059.5:c.153+4_153+5insTATG | ENSP00000458397.1:n.153+4_153+5insTATG | |
| ENST00000578614.1:c.153+4_153+5insTATG | ENSP00000463128.1:n.153+4_153+5insTATG | |
| ENST00000579403.1:n.199+4_199+5insTATG | ||
| ENST00000579855.5:c.153+4_153+5insTATG | ENSP00000463637.1:n.153+4_153+5insTATG | |
| ENST00000580550.5:c.153+4_153+5insTATG | ENSP00000462964.1:n.153+4_153+5insTATG | |
| ENST00000581518.5:c.153+4_153+5insTATG | ENSP00000461916.1:n.153+4_153+5insTATG | |
| ENST00000582991.5:c.153+4_153+5insTATG | ENSP00000464153.1:n.153+4_153+5insTATG | |
| ENST00000584332.6:c.57+4_57+5insTATG | ENSP00000466814.1:n.57+4_57+5insTATG | |
| ENST00000626500.2:c.153+4_153+5insTATG | ENSP00000486283.1:n.153+4_153+5insTATG | |
| ENST00000630662.2:c.-829+4_-829+5insTATG | ENSP00000487353.1:n.-829+4_-829+5insTATG | |
| ENST00000631291.2:c.153+4_153+5insTATG | ENSP00000486085.1:n.153+4_153+5insTATG | |
| NM_000382.2:c.153+4_153+5insTATG | NP_000373.1:n.153+4_153+5insTATG | |
| NM_001031806.1:c.153+4_153+5insTATG | NP_001026976.1:n.153+4_153+5insTATG | |
| XM_011523732.1:c.153+4_153+5insTATG | XP_011522034.1:n.153+4_153+5insTATG | |
| XM_011523733.1:c.153+4_153+5insTATG | XP_011522035.1:n.153+4_153+5insTATG | |
| XM_011523733.2:c.153+4_153+5insTATG | XP_011522035.1:n.153+4_153+5insTATG | |
| XM_017024355.1:c.153+4_153+5insTATG | XP_016879844.1:n.153+4_153+5insTATG | |
| XM_017024356.2:c.153+4_153+5insTATG | XP_016879845.1:n.153+4_153+5insTATG | |
| XM_017024357.1:c.153+4_153+5insTATG | XP_016879846.1:n.153+4_153+5insTATG | |
| XM_017024358.2:c.153+4_153+5insTATG | XP_016879847.1:n.153+4_153+5insTATG | |
| XM_024450652.1:c.-536+4_-536+5insTATG | XP_024306420.1:n.-536+4_-536+5insTATG | |
| NM_000382.3:c.153+4_153+5insTATG MANE Select | NP_000373.1:n.153+4_153+5insTATG | |
| NM_001031806.2:c.153+4_153+5insTATG | NP_001026976.1:n.153+4_153+5insTATG | |
| NM_001369136.1:c.153+4_153+5insTATG | NP_001356065.1:n.153+4_153+5insTATG | |
| NM_001369137.1:c.153+4_153+5insTATG | NP_001356066.1:n.153+4_153+5insTATG | |
| NM_001369138.1:c.153+4_153+5insTATG | NP_001356067.1:n.153+4_153+5insTATG | |
| NM_001369139.1:c.153+4_153+5insTATG | NP_001356068.1:n.153+4_153+5insTATG | |
| NM_001369146.1:c.153+4_153+5insTATG | NP_001356075.1:n.153+4_153+5insTATG | |
| NM_001369148.1:c.-536+4_-536+5insTATG | NP_001356077.1:n.-536+4_-536+5insTATG | |
| NM_001369137.2:c.153+4_153+5insTATG | NP_001356066.1:n.153+4_153+5insTATG | |
| NM_001369138.2:c.153+4_153+5insTATG | NP_001356067.1:n.153+4_153+5insTATG | |
| NM_001369146.2:c.153+4_153+5insTATG | NP_001356075.1:n.153+4_153+5insTATG | |
| NM_001369148.2:c.-536+4_-536+5insTATG | NP_001356077.1:n.-536+4_-536+5insTATG |