Linked Data
ClinVar Variation Id:
97758
ClinVar RCV Id:
RCV000084011
dbSNP Id:
rs104895521
gnomAD v3:
19-54934407-G-GC
gnomAD v4:
19-54934407-G-GC
MyVariant Identifiers:
chr19:g.54934407_54934408insC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.54934407_54934408insC , CM000681.2:g.54934407_54934408insC | GRCh38 |
| NC_000019.8:g.60137587_60137588insC | NCBI36 |
| NG_008056.1:g.18098_18099insG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000592784.6:c.2471+81_2471+82insG (NLRP7) MANE Select | ENSP00000468706.1:n.2471+81_2471+82insG | |
| ENST00000328092.9:c.2387+81_2387+82insG (NLRP7) | ENSP00000329568.5:n.2387+81_2387+82insG | |
| ENST00000340844.6:c.2471+81_2471+82insG (NLRP7) | ENSP00000339491.2:n.2471+81_2471+82insG | |
| ENST00000586379.5:c.2471+81_2471+82insG (NLRP7) | ENSP00000468243.1:n.2471+81_2471+82insG | |
| ENST00000588756.5:c.2471+81_2471+82insG (NLRP7) | ENSP00000467123.1:n.2471+81_2471+82insG | |
| ENST00000590030.5:c.2471+81_2471+82insG (NLRP7) | ENSP00000465520.1:n.2471+81_2471+82insG | |
| ENST00000592784.5:c.2471+81_2471+82insG (NLRP7) | ENSP00000468706.1:n.2471+81_2471+82insG | |
| NM_001127255.1:c.2471+81_2471+82insG (NLRP7) | NP_001120727.1:n.2471+81_2471+82insG | |
| NM_139176.3:c.2387+81_2387+82insG (NLRP7) | NP_631915.2:n.2387+81_2387+82insG | |
| NM_206828.3:c.2471+81_2471+82insG (NLRP7) | NP_996611.2:n.2471+81_2471+82insG | |
| XM_006723075.2:c.2471+81_2471+82insG (NLRP7) | XP_006723138.1:n.2471+81_2471+82insG | |
| XM_006723076.2:c.2471+81_2471+82insG (NLRP7) | XP_006723139.1:n.2471+81_2471+82insG | |
| XM_011526596.1:c.2555+81_2555+82insG (NLRP7) | XP_011524898.1:n.2555+81_2555+82insG | |
| XM_011526597.1:c.2555+81_2555+82insG (NLRP7) | XP_011524899.1:n.2555+81_2555+82insG | |
| XM_011526598.1:c.2555+81_2555+82insG (NLRP7) | XP_011524900.1:n.2555+81_2555+82insG | |
| XM_011526599.1:c.2471+81_2471+82insG (NLRP7) | XP_011524901.1:n.2471+81_2471+82insG | |
| XM_011526600.1:c.2471+81_2471+82insG (NLRP7) | XP_011524902.1:n.2471+81_2471+82insG | |
| XM_011526601.1:c.2555+81_2555+82insG (NLRP7) | XP_011524903.1:n.2555+81_2555+82insG | |
| XM_011527530.1:c.683-3729_683-3728insC (NCR1) | XP_011525832.1:n.683-3729_683-3728insC | |
| XR_935761.1:n.2989+81_2989+82insG (NLRP7) | ||
| XM_006723075.3:c.2471+81_2471+82insG (NLRP7) | XP_006723138.1:n.2471+81_2471+82insG | |
| XM_006723076.3:c.2471+81_2471+82insG (NLRP7) | XP_006723139.1:n.2471+81_2471+82insG | |
| XM_011526596.2:c.2555+81_2555+82insG (NLRP7) | XP_011524898.1:n.2555+81_2555+82insG | |
| XM_011526599.2:c.2471+81_2471+82insG (NLRP7) | XP_011524901.1:n.2471+81_2471+82insG | |
| XM_011526601.2:c.2555+81_2555+82insG (NLRP7) | XP_011524903.1:n.2555+81_2555+82insG | |
| XM_011527530.3:c.683-3729_683-3728insC (NCR1) | XP_011525832.1:n.683-3729_683-3728insC |