Linked Data
ClinVar Variation Id:
256592
dbSNP Id:
rs3838786
ExAC:
11:6411935 TGCTGGC / T
gnomAD v2:
11-6411935-TGCTGGC-T
gnomAD v3:
11-6390705-TGCTGGC-T
gnomAD v4:
11-6390705-TGCTGGC-T
MyVariant Identifiers:
chr11:g.6411966_6411971del (hg19)
chr11:g.6411948_6411953del (hg19)
chr11:g.6411936_6411941del (hg19)
chr11:g.6411966_6411971delGCTGGC (hg19)
chr11:g.6411956_6411961delTGGCGC (hg19)
chr11:g.6390736_6390741del (hg38)
chr11:g.6390718_6390723del (hg38)
chr11:g.6390706_6390711del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390736_6390741del , CM000673.2:g.6390736_6390741del | GRCh38 |
| NC_000011.9:g.6411966_6411971del , CM000673.1:g.6411966_6411971del | GRCh37 |
| NC_000011.8:g.6368542_6368547del | NCBI36 |
| NG_011780.1:g.5312_5317del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.138_143del MANE Select | ENSP00000340409.4:p.Leu47_Ala48del | |
| ENST00000342245.8:c.138_143del | ENSP00000340409.4:p.Leu47_Ala48del | |
| ENST00000527275.5:c.138_143del | ENSP00000435350.1:p.Leu47_Ala48del | |
| ENST00000530395.1:c.-96+97_-96+102del | ENSP00000431479.1:n.-96+97_-96+102del | |
| ENST00000531303.5:c.138_143del | ENSP00000432625.1:p.Leu47_Ala48del | |
| ENST00000533123.5:c.138_143del | ENSP00000435950.1:p.Leu47_Ala48del | |
| ENST00000533196.1:n.297_302del | ||
| ENST00000534405.5:c.138_143del | ENSP00000434353.1:p.Leu47_Ala48del | |
| NM_000543.4:c.138_143del | NP_000534.3:p.Leu47_Ala48del | |
| NM_001007593.2:c.138_143del | NP_001007594.2:p.Leu47_Ala48del | |
| XM_005253075.3:c.138_143del | XP_005253132.1:p.Leu47_Ala48del | |
| XM_011520303.1:c.138_143del | XP_011518605.1:p.Leu47_Ala48del | |
| XM_011520304.1:c.138_143del | XP_011518606.1:p.Leu47_Ala48del | |
| XR_930886.1:n.436_441del | ||
| NM_001318087.1:c.138_143del | NP_001305016.1:p.Leu47_Ala48del | |
| NM_001318088.1:c.-824_-819del | NP_001305017.1:n.-824_-819del | |
| NM_001365135.1:c.138_143del | NP_001352064.1:p.Leu47_Ala48del | |
| NR_027400.2:n.323_328del | ||
| NR_134502.1:n.323_328del | ||
| XM_011520304.2:c.138_143del | XP_011518606.1:p.Leu47_Ala48del | |
| XR_001747940.2:n.263_268del | ||
| XR_002957158.1:n.263_268del | ||
| NM_000543.5:c.138_143del MANE Select | NP_000534.3:p.Leu47_Ala48del | |
| NM_001007593.3:c.138_143del | NP_001007594.2:p.Leu47_Ala48del | |
| NM_001318087.2:c.138_143del | NP_001305016.1:p.Leu47_Ala48del | |
| NM_001318088.2:c.-824_-819del | NP_001305017.1:n.-824_-819del | |
| NM_001365135.2:c.138_143del | NP_001352064.1:p.Leu47_Ala48del | |
| NR_027400.3:n.263_268del | ||
| NR_134502.2:n.263_268del |