Linked Data
dbSNP Id:
rs1445686894
gnomAD v3:
17-43067889-G-GA
gnomAD v4:
17-43067889-G-GA
MyVariant Identifiers:
chr17:g.41219906_41219907insA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43067889_43067890insA , CM000679.2:g.43067889_43067890insA | GRCh38 |
| NC_000017.10:g.41219906_41219907insA , CM000679.1:g.41219906_41219907insA | GRCh37 |
| NC_000017.9:g.38473432_38473433insA | NCBI36 |
| NG_005905.2:g.150094_150095insT , LRG_292:g.150094_150095insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4984-195_4984-194insT | ENSP00000417241.2:n.4984-195_4984-194insT | |
| ENST00000470026.6:c.4987-195_4987-194insT | ENSP00000419274.2:n.4987-195_4987-194insT | |
| ENST00000473961.6:c.4861-195_4861-194insT | ENSP00000420201.2:n.4861-195_4861-194insT | |
| ENST00000476777.6:c.4981-195_4981-194insT | ENSP00000417554.2:n.4981-195_4981-194insT | |
| ENST00000477152.6:c.4909-195_4909-194insT | ENSP00000419988.2:n.4909-195_4909-194insT | |
| ENST00000478531.6:c.1675-195_1675-194insT | ENSP00000420412.2:n.1675-195_1675-194insT | |
| ENST00000489037.2:c.4909-195_4909-194insT | ENSP00000420781.2:n.4909-195_4909-194insT | |
| ENST00000493919.6:c.1537-195_1537-194insT | ENSP00000418819.2:n.1537-195_1537-194insT | |
| ENST00000494123.6:c.4987-195_4987-194insT | ENSP00000419103.2:n.4987-195_4987-194insT | |
| ENST00000497488.2:c.4099-195_4099-194insT | ENSP00000418986.2:n.4099-195_4099-194insT | |
| ENST00000618469.2:c.4987-195_4987-194insT | ENSP00000478114.2:n.4987-195_4987-194insT | |
| ENST00000634433.2:c.4864-195_4864-194insT | ENSP00000489431.2:n.4864-195_4864-194insT | |
| ENST00000644379.2:c.5053-195_5053-194insT | ENSP00000496570.2:n.5053-195_5053-194insT | |
| ENST00000644555.2:c.1537-195_1537-194insT | ENSP00000494614.2:n.1537-195_1537-194insT | |
| ENST00000652672.2:c.4846-195_4846-194insT | ENSP00000498906.2:n.4846-195_4846-194insT | |
| ENST00000484087.6:c.1549-195_1549-194insT | ENSP00000419481.2:n.1549-195_1549-194insT | |
| ENST00000357654.9:c.4987-195_4987-194insT MANE Select | ENSP00000350283.3:n.4987-195_4987-194insT | |
| ENST00000471181.7:c.5050-195_5050-194insT | ENSP00000418960.2:n.5050-195_5050-194insT | |
| ENST00000644379.1:c.1374-195_1374-194insT | ||
| ENST00000352993.7:c.1561-195_1561-194insT | ENSP00000312236.5:n.1561-195_1561-194insT | |
| ENST00000357654.7:c.4987-195_4987-194insT | ENSP00000350283.3:n.4987-195_4987-194insT | |
| ENST00000461221.5:c.*4770-195_*4770-194insT | ENSP00000418548.1:n.*4770-195_*4770-194insT | |
| ENST00000468300.5:c.1675-195_1675-194insT | ENSP00000417148.1:n.1675-195_1675-194insT | |
| ENST00000471181.6:c.5050-195_5050-194insT | ENSP00000418960.2:n.5050-195_5050-194insT | |
| ENST00000472490.1:n.140-195_140-194insT | ||
| ENST00000478531.5:c.1675-195_1675-194insT | ENSP00000420412.1:n.1675-195_1675-194insT | |
| ENST00000484087.5:c.1300-195_1300-194insT | ENSP00000419481.1:n.1300-195_1300-194insT | |
| ENST00000491747.6:c.1675-195_1675-194insT | ENSP00000420705.2:n.1675-195_1675-194insT | |
| ENST00000493795.5:c.4846-195_4846-194insT | ENSP00000418775.1:n.4846-195_4846-194insT | |
| ENST00000493919.5:c.1537-195_1537-194insT | ENSP00000418819.1:n.1537-195_1537-194insT | |
| ENST00000586385.5:c.5-3939_5-3938insT | ENSP00000465818.1:n.5-3939_5-3938insT | |
| ENST00000591534.5:c.460-195_460-194insT | ENSP00000467329.1:n.460-195_460-194insT | |
| ENST00000591849.5:c.-98-17700_-98-17699insT | ENSP00000465347.1:n.-98-17700_-98-17699insT | |
| NM_007294.3:c.4987-195_4987-194insT , LRG_292t1:c.4987-195_4987-194insT | NP_009225.1:n.4987-195_4987-194insT | |
| NM_007297.3:c.4846-195_4846-194insT | NP_009228.2:n.4846-195_4846-194insT | |
| NM_007298.3:c.1675-195_1675-194insT | NP_009229.2:n.1675-195_1675-194insT | |
| NM_007299.3:c.1675-195_1675-194insT | NP_009230.2:n.1675-195_1675-194insT | |
| NM_007300.3:c.5050-195_5050-194insT | NP_009231.2:n.5050-195_5050-194insT | |
| NR_027676.1:n.5123-195_5123-194insT | ||
| NM_007294.4:c.4987-195_4987-194insT MANE Select | NP_009225.1:n.4987-195_4987-194insT | |
| NM_007297.4:c.4846-195_4846-194insT | NP_009228.2:n.4846-195_4846-194insT | |
| NM_007299.4:c.1675-195_1675-194insT | NP_009230.2:n.1675-195_1675-194insT | |
| NM_007300.4:c.5050-195_5050-194insT | NP_009231.2:n.5050-195_5050-194insT | |
| NR_027676.2:n.5164-195_5164-194insT |