Linked Data
ClinVar Variation Id:
1004101
ClinVar RCV Id:
RCV001300754
dbSNP Id:
rs778242525
ExAC:
9:140033976 TCTC / T
gnomAD v2:
9-140033976-TCTC-T
gnomAD v4:
9-137139524-TCTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137139527_137139529del , CM000671.2:g.137139527_137139529del | GRCh38 |
| NC_000009.11:g.140033979_140033981del , CM000671.1:g.140033979_140033981del | GRCh37 |
| NC_000009.10:g.139153800_139153802del | NCBI36 |
| NG_011507.1:g.5371_5373del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371553.8:c.41_43del | ENSP00000360608.3:p.Ser14del | |
| ENST00000371560.5:c.41_43del | ENSP00000360615.3:p.Ser14del | |
| ENST00000371561.8:c.41_43del MANE Select | ENSP00000360616.3:p.Ser14del | |
| ENST00000350902.9:c.41_43del | ENSP00000316915.9:p.Ser14del | |
| ENST00000371546.8:c.41_43del | ENSP00000360601.4:p.Ser14del | |
| ENST00000371550.8:c.41_43del | ENSP00000360605.4:p.Ser14del | |
| ENST00000371553.7:c.41_43del | ENSP00000360608.3:p.Ser14del | |
| ENST00000371555.8:c.41_43del | ENSP00000360610.4:p.Ser14del | |
| ENST00000371559.8:c.41_43del | ENSP00000360614.4:p.Ser14del | |
| ENST00000371560.4:c.41_43del | ENSP00000360615.3:p.Ser14del | |
| ENST00000371561.7:c.41_43del | ENSP00000360616.3:p.Ser14del | |
| ENST00000471122.5:n.118_120del | ||
| NM_000832.6:c.41_43del | NP_000823.4:p.Ser14del | |
| NM_001185090.1:c.41_43del | NP_001172019.1:p.Ser14del | |
| NM_001185091.1:c.41_43del | NP_001172020.1:p.Ser14del | |
| NM_007327.3:c.41_43del | NP_015566.1:p.Ser14del | |
| NM_021569.3:c.41_43del | NP_067544.1:p.Ser14del | |
| XM_005266071.2:c.41_43del | XP_005266128.1:p.Ser14del | |
| XM_005266072.2:c.41_43del | XP_005266129.1:p.Ser14del | |
| XM_005266073.3:c.41_43del | XP_005266130.1:p.Ser14del | |
| XM_011518583.1:c.41_43del | XP_011516885.1:p.Ser14del | |
| XM_005266071.3:c.41_43del | XP_005266128.1:p.Ser14del | |
| XM_005266072.3:c.41_43del | XP_005266129.1:p.Ser14del | |
| XM_005266073.4:c.41_43del | XP_005266130.1:p.Ser14del | |
| XM_011518583.2:c.41_43del | XP_011516885.1:p.Ser14del | |
| NM_007327.4:c.41_43del MANE Select | NP_015566.1:p.Ser14del | |
| NM_000832.7:c.41_43del | NP_000823.4:p.Ser14del | |
| NM_001185090.2:c.41_43del | NP_001172019.1:p.Ser14del | |
| NM_001185091.2:c.41_43del | NP_001172020.1:p.Ser14del | |
| NM_021569.4:c.41_43del | NP_067544.1:p.Ser14del |