Linked Data
dbSNP Id:
rs1473681580
gnomAD v3:
10-87967863-T-TTA
gnomAD v4:
10-87967863-T-TTA
MyVariant Identifiers:
chr10:g.87967863_87967864insTA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87967872_87967873dup , CM000672.2:g.87967872_87967873dup | GRCh38 |
| NC_000010.10:g.89727629_89727630dup , CM000672.1:g.89727629_89727630dup | GRCh37 |
| NC_000010.9:g.89717609_89717610dup | NCBI36 |
| NG_007466.2:g.109434_109435dup , LRG_311:g.109434_109435dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710265.1:c.*2641_*2642dup | ENSP00000518161.1:n.*2641_*2642dup | |
| ENST00000688158.2:n.4347_4348dup | ||
| ENST00000706954.1:c.*2400_*2401dup | ENSP00000516674.1:n.*2400_*2401dup | |
| ENST00000706955.1:c.*3647_*3648dup | ENSP00000516675.1:n.*3647_*3648dup | |
| ENST00000688158.1:c.*3723_*3724dup | ENSP00000509254.1:n.*3723_*3724dup | |
| ENST00000693560.1:c.*2400_*2401dup | ENSP00000509861.1:n.*2400_*2401dup | |
| ENST00000371953.8:c.*2400_*2401dup MANE Select | ENSP00000361021.3:n.*2400_*2401dup | |
| ENST00000371953.7:c.*2400_*2401dup | ENSP00000361021.3:n.*2400_*2401dup | |
| NM_000314.5:c.*2400_*2401dup | NP_000305.3:n.*2400_*2401dup | |
| NM_000314.6:c.*2400_*2401dup | NP_000305.3:n.*2400_*2401dup | |
| NM_001304717.2:c.*2400_*2401dup | NP_001291646.2:n.*2400_*2401dup | |
| NM_001304718.1:c.*2400_*2401dup | NP_001291647.1:n.*2400_*2401dup | |
| XM_006717926.2:c.*2400_*2401dup | XP_006717989.1:n.*2400_*2401dup | |
| XM_011539982.1:c.*2400_*2401dup | XP_011538284.1:n.*2400_*2401dup | |
| XR_945791.1:n.4182_4183dup | ||
| NM_000314.7:c.*2400_*2401dup | NP_000305.3:n.*2400_*2401dup | |
| NM_001304717.5:c.*2400_*2401dup | NP_001291646.4:n.*2400_*2401dup | |
| NM_001304718.2:c.*2400_*2401dup | NP_001291647.1:n.*2400_*2401dup | |
| NM_000314.8:c.*2400_*2401dup MANE Select | NP_000305.3:n.*2400_*2401dup |