Linked Data
dbSNP Id:
rs982712218
MyVariant Identifiers:
chr13:g.23942381_23942382insGCTATACACT (hg19)
chr13:g.23368242_23368243insGCTATACACT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23368255_23368264dup , CM000675.2:g.23368255_23368264dup | GRCh38 |
| NC_000013.10:g.23942394_23942403dup , CM000675.1:g.23942394_23942403dup | GRCh37 |
| NC_000013.9:g.22840394_22840403dup | NCBI36 |
| NG_012342.1:g.70451_70460dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682244.1:n.918+150_918+159dup | ||
| ENST00000682354.1:n.1110+150_1110+159dup | ||
| ENST00000682775.1:c.345+150_345+159dup | ENSP00000508399.1:n.345+150_345+159dup | |
| ENST00000682944.1:c.345+150_345+159dup | ENSP00000507173.1:n.345+150_345+159dup | |
| ENST00000683154.1:n.483+150_483+159dup | ||
| ENST00000683210.1:c.345+150_345+159dup | ENSP00000506739.1:n.345+150_345+159dup | |
| ENST00000683270.1:c.336+150_336+159dup | ENSP00000507624.1:n.336+150_336+159dup | |
| ENST00000683367.1:c.336+150_336+159dup | ENSP00000507780.1:n.336+150_336+159dup | |
| ENST00000683489.1:c.345+150_345+159dup | ENSP00000508403.1:n.345+150_345+159dup | |
| ENST00000683680.1:c.345+150_345+159dup | ENSP00000507223.1:n.345+150_345+159dup | |
| ENST00000684053.1:n.462+150_462+159dup | ||
| ENST00000684163.1:c.336+150_336+159dup | ENSP00000508262.1:n.336+150_336+159dup | |
| ENST00000684196.1:n.2702+150_2702+159dup | ||
| ENST00000684325.1:c.345+150_345+159dup | ENSP00000508121.1:n.345+150_345+159dup | |
| ENST00000684385.1:c.345+150_345+159dup | ENSP00000507855.1:n.345+150_345+159dup | |
| ENST00000684497.1:c.345+150_345+159dup | ENSP00000507057.1:n.345+150_345+159dup | |
| ENST00000382292.9:c.345+150_345+159dup MANE Select | ENSP00000371729.3:n.345+150_345+159dup | |
| ENST00000423156.2:c.345+150_345+159dup | ENSP00000390925.2:n.345+150_345+159dup | |
| ENST00000455470.6:c.345+150_345+159dup | ENSP00000406565.2:n.345+150_345+159dup | |
| ENST00000382292.7:c.345+150_345+159dup | ENSP00000371729.3:n.345+150_345+159dup | |
| ENST00000382298.7:c.345+150_345+159dup | ENSP00000371735.3:n.345+150_345+159dup | |
| ENST00000402364.1:c.-1906+150_-1906+159dup | ENSP00000385844.1:n.-1906+150_-1906+159dup | |
| ENST00000455470.5:c.43+150_43+159dup | ||
| NM_001278055.1:c.-97+150_-97+159dup | NP_001264984.1:n.-97+150_-97+159dup | |
| NM_014363.5:c.345+150_345+159dup | NP_055178.3:n.345+150_345+159dup | |
| XM_005266338.1:c.345+150_345+159dup | XP_005266395.1:n.345+150_345+159dup | |
| XM_011535038.1:c.369+150_369+159dup | XP_011533340.1:n.369+150_369+159dup | |
| XM_011535039.1:c.336+150_336+159dup | XP_011533341.1:n.336+150_336+159dup | |
| XM_005266338.2:c.345+150_345+159dup | XP_005266395.1:n.345+150_345+159dup | |
| XM_011535039.2:c.336+150_336+159dup | XP_011533341.1:n.336+150_336+159dup | |
| XM_017020539.1:c.336+150_336+159dup | XP_016876028.1:n.336+150_336+159dup | |
| XM_024449337.1:c.345+150_345+159dup | XP_024305105.1:n.345+150_345+159dup | |
| NM_014363.6:c.345+150_345+159dup MANE Select | NP_055178.3:n.345+150_345+159dup | |
| NM_001278055.2:c.-97+150_-97+159dup | NP_001264984.1:n.-97+150_-97+159dup |