Linked Data
ClinVar Variation Id:
550227
ClinVar RCV Id:
RCV000664918
dbSNP Id:
rs1554767735
MyVariant Identifiers:
chr8:g.99391642del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99391642del , CM000670.2:g.99391642del | GRCh38 |
| NC_000008.10:g.100403870del , CM000670.1:g.100403870del | GRCh37 |
| NC_000008.9:g.100473046del | NCBI36 |
| NG_007098.2:g.383377del , LRG_351:g.383377del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355155.6:c.3017del | ENSP00000347281.2:p.Lys1006SerfsTer15 | |
| ENST00000682145.1:n.2897del | ||
| ENST00000682153.1:c.3020del | ENSP00000507923.1:p.Lys1007SerfsTer15 | |
| ENST00000682234.1:c.3020del | ENSP00000508225.1:p.Lys1007SerfsTer15 | |
| ENST00000682358.1:n.3090del | ||
| ENST00000683334.1:c.3020del | ENSP00000507369.1:p.Lys1007SerfsTer15 | |
| ENST00000683486.1:n.3086del | ||
| ENST00000683619.1:n.3192del | ||
| ENST00000683869.1:n.3101del | ||
| ENST00000357162.7:c.3020del MANE Select | ENSP00000349685.2:p.Lys1007SerfsTer15 | |
| ENST00000358544.7:c.3020del MANE Plus Clinical | ENSP00000351346.2:p.Lys1007SerfsTer15 | |
| ENST00000357162.6:c.3020del | ENSP00000349685.2:p.Lys1007SerfsTer15 | |
| ENST00000358544.6:c.3020del | ENSP00000351346.2:p.Lys1007SerfsTer15 | |
| ENST00000496144.5:c.3020del | ENSP00000430900.1:p.Lys1007SerfsTer15 | |
| ENST00000521037.1:n.191del | ||
| ENST00000522802.5:n.242del | ||
| NM_017890.4:c.3020del , LRG_351t1:c.3020del | NP_060360.3:p.Lys1007SerfsTer15 | |
| NM_152564.4:c.3020del , LRG_351t2:c.3020del | NP_689777.3:p.Lys1007SerfsTer15 | |
| XM_005250800.2:c.3020del | XP_005250857.1:p.Lys1007SerfsTer15 | |
| XM_005250801.3:c.3020del | XP_005250858.1:p.Lys1007SerfsTer15 | |
| XM_006716510.2:c.3020del | XP_006716573.1:p.Lys1007SerfsTer15 | |
| XM_011516848.1:c.3017del | XP_011515150.1:p.Lys1006SerfsTer15 | |
| XM_011516849.1:c.3020del | XP_011515151.1:p.Lys1007SerfsTer15 | |
| XM_011516850.1:c.2642del | XP_011515152.1:p.Lys881SerfsTer15 | |
| XM_011516851.1:c.-111del | XP_011515153.1:n.-111del | |
| XM_011516853.1:c.3020del | XP_011515155.1:p.Lys1007SerfsTer15 | |
| XM_011516855.1:c.3020del | XP_011515157.1:p.Lys1007SerfsTer15 | |
| XM_011516856.1:c.3020del | XP_011515158.1:p.Lys1007SerfsTer15 | |
| XM_011516857.1:c.3020del | XP_011515159.1:p.Lys1007SerfsTer15 | |
| XM_011516858.1:c.3020del | XP_011515160.1:p.Lys1007SerfsTer15 | |
| XM_011516859.1:c.3020del | XP_011515161.1:p.Lys1007SerfsTer15 | |
| XM_011516860.1:c.3020del | XP_011515162.1:p.Lys1007SerfsTer15 | |
| XM_011516861.1:c.3020del | XP_011515163.1:p.Lys1007SerfsTer15 | |
| XR_928301.1:n.3123del | ||
| XR_928302.1:n.3123del | ||
| XR_928303.1:n.3123del | ||
| XR_928304.1:n.3123del | ||
| XM_005250800.3:c.3020del | XP_005250857.1:p.Lys1007SerfsTer15 | |
| XM_005250801.5:c.3020del | XP_005250858.1:p.Lys1007SerfsTer15 | |
| XM_006716510.3:c.3020del | XP_006716573.1:p.Lys1007SerfsTer15 | |
| XM_011516848.2:c.3017del | XP_011515150.1:p.Lys1006SerfsTer15 | |
| XM_011516849.2:c.3020del | XP_011515151.1:p.Lys1007SerfsTer15 | |
| XM_011516850.2:c.2642del | XP_011515152.1:p.Lys881SerfsTer15 | |
| XM_011516851.2:c.-111del | XP_011515153.1:n.-111del | |
| XM_011516853.2:c.3020del | XP_011515155.1:p.Lys1007SerfsTer15 | |
| XM_011516859.2:c.3020del | XP_011515161.1:p.Lys1007SerfsTer15 | |
| XM_017013109.1:c.2825del | XP_016868598.1:p.Lys942SerfsTer15 | |
| XM_024447074.1:c.1805del | XP_024302842.1:p.Lys602SerfsTer15 | |
| XM_024447075.1:c.3020del | XP_024302843.1:p.Lys1007SerfsTer15 | |
| XR_001745481.1:n.3123del | ||
| XR_001745482.2:n.3123del | ||
| XR_001745484.2:n.3123del | ||
| XR_002956601.1:n.3120del | ||
| XR_002956602.1:n.3123del | ||
| XR_928302.2:n.3123del | ||
| NM_017890.5:c.3020del MANE Plus Clinical | NP_060360.3:p.Lys1007SerfsTer15 | |
| NM_152564.5:c.3020del MANE Select | NP_689777.3:p.Lys1007SerfsTer15 |