Linked Data
dbSNP Id:
rs772233075
gnomAD v2:
19-38993409-AGGGGCAGGG-A
gnomAD v4:
19-38502769-AGGGGCAGGG-A
MyVariant Identifiers:
chr19:g.38993411_38993424delinsCAGGG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38502771_38502779del , CM000681.2:g.38502771_38502779del | GRCh38 |
| NC_000019.9:g.38993411_38993419del , CM000681.1:g.38993411_38993419del | GRCh37 |
| NC_000019.8:g.43685251_43685259del | NCBI36 |
| NG_008866.1:g.74072_74080del , LRG_766:g.74072_74080del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.7835+44_7835+52del | ENSP00000471601.2:n.7835+44_7835+52del | |
| ENST00000359596.8:c.7835+44_7835+52del MANE Select | ENSP00000352608.2:n.7835+44_7835+52del | |
| ENST00000355481.8:c.7835+44_7835+52del | ENSP00000347667.3:n.7835+44_7835+52del | |
| ENST00000359596.7:c.7835+44_7835+52del | ENSP00000352608.2:n.7835+44_7835+52del | |
| ENST00000360985.7:c.7832+44_7832+52del | ENSP00000354254.4:n.7832+44_7832+52del | |
| ENST00000594335.5:c.1287+44_1287+52del | ||
| NM_000540.2:c.7835+44_7835+52del , LRG_766t1:c.7835+44_7835+52del | NP_000531.2:n.7835+44_7835+52del | |
| NM_001042723.1:c.7835+44_7835+52del | NP_001036188.1:n.7835+44_7835+52del | |
| XM_006723317.1:c.7835+44_7835+52del | XP_006723380.1:n.7835+44_7835+52del | |
| XM_006723319.1:c.7835+44_7835+52del | XP_006723382.1:n.7835+44_7835+52del | |
| XM_011527204.1:c.7832+44_7832+52del | XP_011525506.1:n.7832+44_7832+52del | |
| XM_011527205.1:c.7835+44_7835+52del | XP_011525507.1:n.7835+44_7835+52del | |
| XM_006723317.2:c.7835+44_7835+52del | XP_006723380.1:n.7835+44_7835+52del | |
| XM_006723319.2:c.7835+44_7835+52del | XP_006723382.1:n.7835+44_7835+52del | |
| XM_011527205.2:c.7835+44_7835+52del | XP_011525507.1:n.7835+44_7835+52del | |
| XR_001753735.1:n.7918+44_7918+52del | ||
| NM_000540.3:c.7835+44_7835+52del MANE Select | NP_000531.2:n.7835+44_7835+52del | |
| NM_001042723.2:c.7835+44_7835+52del | NP_001036188.1:n.7835+44_7835+52del |