Linked Data
dbSNP Id:
rs1392835132
gnomAD v3:
10-87967456-ATAGAG-A
gnomAD v4:
10-87967456-ATAGAG-A
MyVariant Identifiers:
chr10:g.87967457_87967461del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87967459_87967463del , CM000672.2:g.87967459_87967463del | GRCh38 |
| NC_000010.10:g.89727216_89727220del , CM000672.1:g.89727216_89727220del | GRCh37 |
| NC_000010.9:g.89717196_89717200del | NCBI36 |
| NG_007466.2:g.109021_109025del , LRG_311:g.109021_109025del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710265.1:c.*2228_*2232del | ENSP00000518161.1:n.*2228_*2232del | |
| ENST00000688158.2:n.3934_3938del | ||
| ENST00000706954.1:c.*1987_*1991del | ENSP00000516674.1:n.*1987_*1991del | |
| ENST00000706955.1:c.*3234_*3238del | ENSP00000516675.1:n.*3234_*3238del | |
| ENST00000688158.1:c.*3310_*3314del | ENSP00000509254.1:n.*3310_*3314del | |
| ENST00000693560.1:c.*1987_*1991del | ENSP00000509861.1:n.*1987_*1991del | |
| ENST00000371953.8:c.*1987_*1991del MANE Select | ENSP00000361021.3:n.*1987_*1991del | |
| ENST00000371953.7:c.*1987_*1991del | ENSP00000361021.3:n.*1987_*1991del | |
| NM_000314.5:c.*1987_*1991del | NP_000305.3:n.*1987_*1991del | |
| NM_000314.6:c.*1987_*1991del | NP_000305.3:n.*1987_*1991del | |
| NM_001304717.2:c.*1987_*1991del | NP_001291646.2:n.*1987_*1991del | |
| NM_001304718.1:c.*1987_*1991del | NP_001291647.1:n.*1987_*1991del | |
| XM_006717926.2:c.*1987_*1991del | XP_006717989.1:n.*1987_*1991del | |
| XM_011539982.1:c.*1987_*1991del | XP_011538284.1:n.*1987_*1991del | |
| XR_945791.1:n.3769_3773del | ||
| NM_000314.7:c.*1987_*1991del | NP_000305.3:n.*1987_*1991del | |
| NM_001304717.5:c.*1987_*1991del | NP_001291646.4:n.*1987_*1991del | |
| NM_001304718.2:c.*1987_*1991del | NP_001291647.1:n.*1987_*1991del | |
| NM_000314.8:c.*1987_*1991del MANE Select | NP_000305.3:n.*1987_*1991del |