Linked Data
ClinVar Variation Id:
37545
dbSNP Id:
rs80357848
gnomAD v3:
17-43091766-G-GT
gnomAD v4:
17-43091766-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43091768dup , CM000679.2:g.43091768dup | GRCh38 |
| NC_000017.10:g.41243785dup , CM000679.1:g.41243785dup | GRCh37 |
| NC_000017.9:g.38497311dup | NCBI36 |
| NG_005905.2:g.126217dup , LRG_292:g.126217dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.3828dup | ||
| ENST00000461574.2:c.3764dup | ENSP00000417241.2:p.Asn1255LysfsTer12 | |
| ENST00000470026.6:c.3764dup | ENSP00000419274.2:p.Asn1255LysfsTer12 | |
| ENST00000473961.6:c.3638dup | ENSP00000420201.2:p.Asn1213LysfsTer12 | |
| ENST00000476777.6:c.3761dup | ENSP00000417554.2:p.Asn1254LysfsTer12 | |
| ENST00000477152.6:c.3686dup | ENSP00000419988.2:p.Asn1229LysfsTer12 | |
| ENST00000478531.6:c.785-735dup | ENSP00000420412.2:n.785-735dup | |
| ENST00000489037.2:c.3686dup | ENSP00000420781.2:p.Asn1229LysfsTer12 | |
| ENST00000493919.6:c.647-735dup | ENSP00000418819.2:n.647-735dup | |
| ENST00000494123.6:c.3764dup | ENSP00000419103.2:p.Asn1255LysfsTer12 | |
| ENST00000497488.2:c.2876dup | ENSP00000418986.2:p.Asn959LysfsTer12 | |
| ENST00000618469.2:c.3764dup | ENSP00000478114.2:p.Asn1255LysfsTer12 | |
| ENST00000634433.2:c.3641dup | ENSP00000489431.2:p.Asn1214LysfsTer12 | |
| ENST00000644379.2:c.3764dup | ENSP00000496570.2:p.Asn1255LysfsTer12 | |
| ENST00000644555.2:c.647-735dup | ENSP00000494614.2:n.647-735dup | |
| ENST00000652672.2:c.3623dup | ENSP00000498906.2:p.Asn1208LysfsTer12 | |
| ENST00000484087.6:c.665-735dup | ENSP00000419481.2:n.665-735dup | |
| ENST00000700182.1:c.707-735dup | ENSP00000514849.1:n.707-735dup | |
| ENST00000357654.9:c.3764dup MANE Select | ENSP00000350283.3:p.Asn1255LysfsTer12 | |
| ENST00000471181.7:c.3764dup | ENSP00000418960.2:p.Asn1255LysfsTer12 | |
| ENST00000644379.1:c.85dup | ||
| ENST00000352993.7:c.671-735dup | ENSP00000312236.5:n.671-735dup | |
| ENST00000354071.7:c.3764dup | ENSP00000326002.7:p.Asn1255LysfsTer12 | |
| ENST00000357654.7:c.3764dup | ENSP00000350283.3:p.Asn1255LysfsTer12 | |
| ENST00000461221.5:c.*3547dup | ENSP00000418548.1:n.*3547dup | |
| ENST00000461574.1:c.58dup | ||
| ENST00000468300.5:c.788-735dup | ENSP00000417148.1:n.788-735dup | |
| ENST00000471181.6:c.3764dup | ENSP00000418960.2:p.Asn1255LysfsTer12 | |
| ENST00000478531.5:c.785-735dup | ENSP00000420412.1:n.785-735dup | |
| ENST00000484087.5:c.410-735dup | ENSP00000419481.1:n.410-735dup | |
| ENST00000487825.5:c.413-735dup | ENSP00000418212.1:n.413-735dup | |
| ENST00000491747.6:c.788-735dup | ENSP00000420705.2:n.788-735dup | |
| ENST00000493795.5:c.3623dup | ENSP00000418775.1:p.Asn1208LysfsTer12 | |
| ENST00000493919.5:c.647-735dup | ENSP00000418819.1:n.647-735dup | |
| ENST00000586385.5:c.5-27816dup | ENSP00000465818.1:n.5-27816dup | |
| ENST00000591534.5:c.-43-17246dup | ENSP00000467329.1:n.-43-17246dup | |
| ENST00000591849.5:c.-99+33504dup | ENSP00000465347.1:n.-99+33504dup | |
| NM_007294.3:c.3764dup , LRG_292t1:c.3764dup | NP_009225.1:p.Asn1255LysfsTer12 | |
| NM_007297.3:c.3623dup | NP_009228.2:p.Asn1208LysfsTer12 | |
| NM_007298.3:c.788-735dup | NP_009229.2:n.788-735dup | |
| NM_007299.3:c.788-735dup | NP_009230.2:n.788-735dup | |
| NM_007300.3:c.3764dup | NP_009231.2:p.Asn1255LysfsTer12 | |
| NR_027676.1:n.3900dup | ||
| NM_007294.4:c.3764dup MANE Select | NP_009225.1:p.Asn1255LysfsTer12 | |
| NM_007297.4:c.3623dup | NP_009228.2:p.Asn1208LysfsTer12 | |
| NM_007299.4:c.788-735dup | NP_009230.2:n.788-735dup | |
| NM_007300.4:c.3764dup | NP_009231.2:p.Asn1255LysfsTer12 | |
| NR_027676.2:n.3941dup |