Linked Data
dbSNP Id:
rs753568011
ExAC:
5:131892971 CT / C
gnomAD v2:
5-131892971-CT-C
gnomAD v3:
5-132557279-CT-C
gnomAD v4:
5-132557279-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132557282del , CM000667.2:g.132557282del | GRCh38 |
| NC_000005.9:g.131892974del , CM000667.1:g.131892974del | GRCh37 |
| NC_000005.8:g.131920873del | NCBI36 |
| NG_021151.1:g.5359del | |
| NG_021151.2:g.5306del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.-43del MANE Select | ENSP00000368100.4:n.-43del | |
| ENST00000638452.2:c.-168-2002del | ENSP00000492349.2:n.-168-2002del | |
| ENST00000638504.1:n.207-2002del | ||
| ENST00000638568.2:c.-169+809del | ENSP00000491158.2:n.-169+809del | |
| ENST00000639899.1:n.290-2002del | ||
| ENST00000640655.2:c.-168-2002del | ENSP00000491596.2:n.-168-2002del | |
| ENST00000651160.1:c.-43del | ENSP00000498829.1:n.-43del | |
| ENST00000651541.1:c.-169+273del | ENSP00000498795.1:n.-169+273del | |
| ENST00000651658.1:n.26del | ||
| ENST00000651723.1:c.-43del | ENSP00000498237.1:n.-43del | |
| ENST00000652016.1:c.-43del | ENSP00000498267.1:n.-43del | |
| ENST00000652485.1:c.-43del | ENSP00000498973.1:n.-43del | |
| ENST00000378823.7:c.-43del | ENSP00000368100.4:n.-43del | |
| ENST00000416135.5:c.-169+809del | ENSP00000389515.1:n.-169+809del | |
| ENST00000423956.5:c.-43del | ENSP00000390971.1:n.-43del | |
| ENST00000453394.5:c.-43del | ENSP00000400049.1:n.-43del | |
| ENST00000533482.5:c.-43del | ENSP00000431225.1:n.-43del | |
| NM_005732.3:c.-43del | NP_005723.2:n.-43del | |
| NM_005732.4:c.-43del MANE Select | NP_005723.2:n.-43del |