Linked Data
ClinVar Variation Id:
561102
ClinVar RCV Id:
RCV000680088
dbSNP Id:
rs1568501473
MyVariant Identifiers:
chr19:g.38499908del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38499908del , CM000681.2:g.38499908del | GRCh38 |
| NC_000019.9:g.38990548del , CM000681.1:g.38990548del | GRCh37 |
| NC_000019.8:g.43682388del | NCBI36 |
| NG_008866.1:g.71209del , LRG_766:g.71209del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000599547.6:c.7215del | ENSP00000471601.2:p.Phe2406LeufsTer24 | |
| ENST00000359596.8:c.7215del MANE Select | ENSP00000352608.2:p.Phe2406LeufsTer24 | |
| ENST00000355481.8:c.7215del | ENSP00000347667.3:p.Phe2406LeufsTer24 | |
| ENST00000359596.7:c.7215del | ENSP00000352608.2:p.Phe2406LeufsTer24 | |
| ENST00000360985.7:c.7212del | ENSP00000354254.4:p.Phe2405LeufsTer24 | |
| ENST00000594335.5:c.667del | ||
| NM_000540.2:c.7215del , LRG_766t1:c.7215del | NP_000531.2:p.Phe2406LeufsTer24 | |
| NM_001042723.1:c.7215del | NP_001036188.1:p.Phe2406LeufsTer24 | |
| XM_006723317.1:c.7215del | XP_006723380.1:p.Phe2406LeufsTer24 | |
| XM_006723319.1:c.7215del | XP_006723382.1:p.Phe2406LeufsTer24 | |
| XM_011527204.1:c.7212del | XP_011525506.1:p.Phe2405LeufsTer24 | |
| XM_011527205.1:c.7215del | XP_011525507.1:p.Phe2406LeufsTer24 | |
| XM_006723317.2:c.7215del | XP_006723380.1:p.Phe2406LeufsTer24 | |
| XM_006723319.2:c.7215del | XP_006723382.1:p.Phe2406LeufsTer24 | |
| XM_011527205.2:c.7215del | XP_011525507.1:p.Phe2406LeufsTer24 | |
| XR_001753735.1:n.7298del | ||
| NM_000540.3:c.7215del MANE Select | NP_000531.2:p.Phe2406LeufsTer24 | |
| NM_001042723.2:c.7215del | NP_001036188.1:p.Phe2406LeufsTer24 |