Linked Data
dbSNP Id:
rs748077679
ExAC:
9:125143637 A / AC
gnomAD v2:
9-125143637-A-AC
gnomAD v3:
9-122381358-A-AC
gnomAD v4:
9-122381358-A-AC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.122381364dup , CM000671.2:g.122381364dup | GRCh38 |
| NC_000009.11:g.125143643dup , CM000671.1:g.125143643dup | GRCh37 |
| NC_000009.10:g.124183464dup | NCBI36 |
| NG_032900.1:g.15415dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362012.7:c.497-7dup MANE Select | ENSP00000354612.2:n.497-7dup | |
| ENST00000373698.7:c.170-7dup | ENSP00000362802.5:n.170-7dup | |
| ENST00000426608.6:c.313-132dup | ENSP00000411606.2:n.313-132dup | |
| ENST00000540753.6:c.422-7dup | ENSP00000437709.1:n.422-7dup | |
| ENST00000619306.5:c.353-7dup | ENSP00000483540.2:n.353-7dup | |
| ENST00000643576.1:n.591-7dup | ||
| ENST00000643810.1:c.170-7dup | ENSP00000494717.1:n.170-7dup | |
| ENST00000645132.1:n.519+2791dup | ||
| ENST00000647067.1:c.*342-7dup | ENSP00000495728.1:n.*342-7dup | |
| ENST00000223423.8:c.497-7dup | ENSP00000223423.4:n.497-7dup | |
| ENST00000362012.6:c.497-7dup | ENSP00000354612.2:n.497-7dup | |
| ENST00000373698.6:c.170-7dup | ENSP00000362802.5:n.170-7dup | |
| ENST00000426608.5:c.304-132dup | ENSP00000411606.1:n.304-132dup | |
| ENST00000540753.5:c.422-7dup | ENSP00000437709.1:n.422-7dup | |
| ENST00000614910.4:c.353-7dup | ENSP00000484800.1:n.353-7dup | |
| ENST00000619306.4:c.590-7dup | ENSP00000483540.1:n.590-7dup | |
| NM_000962.3:c.497-7dup | NP_000953.2:n.497-7dup | |
| NM_001271164.1:c.353-7dup | NP_001258093.1:n.353-7dup | |
| NM_001271165.1:c.170-7dup | NP_001258094.1:n.170-7dup | |
| NM_001271166.1:c.170-7dup | NP_001258095.1:n.170-7dup | |
| NM_001271367.1:c.170-7dup | NP_001258296.1:n.170-7dup | |
| NM_001271368.1:c.422-7dup | NP_001258297.1:n.422-7dup | |
| NM_080591.2:c.497-7dup | NP_542158.1:n.497-7dup | |
| XM_005252105.2:c.422-7dup | XP_005252162.1:n.422-7dup | |
| XM_011518875.1:c.422-7dup | XP_011517177.1:n.422-7dup | |
| XM_011518876.1:c.170-7dup | XP_011517178.1:n.170-7dup | |
| XM_005252105.3:c.422-7dup | XP_005252162.1:n.422-7dup | |
| XM_011518875.2:c.422-7dup | XP_011517177.1:n.422-7dup | |
| XM_011518876.2:c.170-7dup | XP_011517178.1:n.170-7dup | |
| XM_024447614.1:c.170-7dup | XP_024303382.1:n.170-7dup | |
| XM_024447615.1:c.170-7dup | XP_024303383.1:n.170-7dup | |
| NM_000962.4:c.497-7dup MANE Select | NP_000953.2:n.497-7dup | |
| NM_001271164.2:c.353-7dup | NP_001258093.1:n.353-7dup | |
| NM_001271165.2:c.170-7dup | NP_001258094.1:n.170-7dup | |
| NM_001271166.2:c.170-7dup | NP_001258095.1:n.170-7dup | |
| NM_001271367.2:c.170-7dup | NP_001258296.1:n.170-7dup | |
| NM_001271368.2:c.422-7dup | NP_001258297.1:n.422-7dup | |
| NM_080591.3:c.497-7dup | NP_542158.1:n.497-7dup |