Linked Data
ClinVar Variation Id:
229935
dbSNP Id:
rs587781979
gnomAD v2:
2-215674253-A-ATCCTCGGCTGCCGGT
gnomAD v3:
2-214809529-A-ATCCTCGGCTGCCGGT
gnomAD v4:
2-214809529-A-ATCCTCGGCTGCCGGT
MyVariant Identifiers:
chr2:g.215674254_215674268dupTCCTCGGCTGCCGGT (hg19)
chr2:g.215674268_215674269insTCCTCGGCTGCCGGT (hg19)
chr2:g.215674253_215674254insTCCTCGGCTGCCGGT (hg19)
chr2:g.214809530_214809544dupTCCTCGGCTGCCGGT (hg38)
chr2:g.214809544_214809545insTCCTCGGCTGCCGGT (hg38)
chr2:g.214809529_214809530insTCCTCGGCTGCCGGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214809543_214809557dup , CM000664.2:g.214809543_214809557dup | GRCh38 |
| NC_000002.11:g.215674267_215674281dup , CM000664.1:g.215674267_215674281dup | GRCh37 |
| NC_000002.10:g.215382512_215382526dup | NCBI36 |
| NG_012047.2:g.5161_5175dup | |
| NG_012047.3:g.5168_5182dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.26_40dup MANE Select | ENSP00000260947.4:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000421162.2:c.26_40dup | ENSP00000392245.2:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000613192.2:c.26_40dup | ENSP00000483275.2:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000613374.5:c.26_40dup | ENSP00000484464.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000613706.5:c.26_40dup | ENSP00000484976.2:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000617164.5:c.26_40dup | ENSP00000480470.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000619009.5:c.26_40dup | ENSP00000482293.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000260947.8:c.26_40dup | ENSP00000260947.4:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000421162.1:c.26_40dup | ENSP00000392245.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000455743.5:c.26_40dup | ENSP00000412186.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000471787.1:n.127_141dup | ||
| ENST00000479904.1:n.117_131dup | ||
| ENST00000613192.1:c.-60_-46dup | ENSP00000483275.1:n.-60_-46dup | |
| ENST00000613374.4:c.26_40dup | ENSP00000484464.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000613706.4:c.26_40dup | ENSP00000484976.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000617164.4:c.26_40dup | ENSP00000480470.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000619009.4:c.26_40dup | ENSP00000482293.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| ENST00000620057.4:c.26_40dup | ENSP00000481988.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_000465.3:c.26_40dup | NP_000456.2:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282543.1:c.26_40dup | NP_001269472.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282545.1:c.26_40dup | NP_001269474.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282548.1:c.26_40dup | NP_001269477.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282549.1:c.26_40dup | NP_001269478.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NR_104212.1:n.168_182dup | ||
| NR_104215.1:n.168_182dup | ||
| NR_104216.1:n.168_182dup | ||
| XM_011511568.1:c.26_40dup | XP_011509870.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| XM_017004613.1:c.26_40dup | XP_016860102.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| XM_017004614.1:c.26_40dup | XP_016860103.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| XR_002959322.1:n.117_131dup | ||
| NM_000465.4:c.26_40dup MANE Select | NP_000456.2:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282543.2:c.26_40dup | NP_001269472.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282545.2:c.26_40dup | NP_001269474.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282548.2:c.26_40dup | NP_001269477.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NM_001282549.2:c.26_40dup | NP_001269478.1:p.Arg13_Ile14insAsnArgGlnProArg | |
| NR_104212.2:n.140_154dup | ||
| NR_104215.2:n.140_154dup | ||
| NR_104216.2:n.140_154dup |