Linked Data
dbSNP Id:
rs1174739171
gnomAD v2:
15-28356808-G-GACGC
gnomAD v3:
15-28111662-G-GACGC
gnomAD v4:
15-28111662-G-GACGC
MyVariant Identifiers:
chr15:g.28356808_28356809insACGC (hg19)
chr15:g.28111662_28111663insACGC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.28111663_28111666dup , CM000677.2:g.28111663_28111666dup | GRCh38 |
| NC_000015.9:g.28356809_28356812dup , CM000677.1:g.28356809_28356812dup | GRCh37 |
| NC_000015.8:g.26030404_26030407dup | NCBI36 |
| NG_016355.1:g.215484_215487dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261609.13:c.*97_*100dup MANE Select | ENSP00000261609.8:n.*97_*100dup | |
| ENST00000650509.1:c.6081_6084dup | ENSP00000496936.1:n.6081_6084dup | |
| ENST00000261609.11:c.*97_*100dup | ENSP00000261609.7:n.*97_*100dup | |
| ENST00000566635.5:n.1727_1730dup | ||
| NM_004667.5:c.*97_*100dup | NP_004658.3:n.*97_*100dup | |
| XM_005268276.3:c.*97_*100dup | XP_005268333.1:n.*97_*100dup | |
| XM_005268277.3:c.*97_*100dup | XP_005268334.1:n.*97_*100dup | |
| XM_006720726.2:c.*97_*100dup | XP_006720789.1:n.*97_*100dup | |
| XM_006720727.2:c.*97_*100dup | XP_006720790.1:n.*97_*100dup | |
| XM_011522131.1:c.*97_*100dup | XP_011520433.1:n.*97_*100dup | |
| XM_011522132.1:c.*97_*100dup | XP_011520434.1:n.*97_*100dup | |
| XM_011522133.1:c.*97_*100dup | XP_011520435.1:n.*97_*100dup | |
| XM_011522134.1:c.*97_*100dup | XP_011520436.1:n.*97_*100dup | |
| XM_005268276.5:c.*97_*100dup | XP_005268333.1:n.*97_*100dup | |
| XM_006720726.3:c.*97_*100dup | XP_006720789.1:n.*97_*100dup | |
| XM_006720727.3:c.*97_*100dup | XP_006720790.1:n.*97_*100dup | |
| XM_017022695.1:c.*97_*100dup | XP_016878184.1:n.*97_*100dup | |
| XM_017022696.1:c.*97_*100dup | XP_016878185.1:n.*97_*100dup | |
| XM_017022697.1:c.*97_*100dup | XP_016878186.1:n.*97_*100dup | |
| XM_017022698.1:c.*97_*100dup | XP_016878187.1:n.*97_*100dup | |
| NM_004667.6:c.*97_*100dup MANE Select | NP_004658.3:n.*97_*100dup |