Linked Data
ClinVar Variation Id:
418318
dbSNP Id:
rs767894453
ExAC:
2:48010529 G / GCTGGGC
gnomAD v2:
2-48010529-G-GCTGGGC
gnomAD v4:
2-47783390-G-GCTGGGC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47783398_47783403dup , CM000664.2:g.47783398_47783403dup | GRCh38 |
| NC_000002.11:g.48010537_48010542dup , CM000664.1:g.48010537_48010542dup | GRCh37 |
| NC_000002.10:g.47864041_47864046dup | NCBI36 |
| NG_007111.1:g.5252_5257dup , LRG_219:g.5252_5257dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700004.2:c.165_170dup | ENSP00000514752.2:p.Pro57_Arg58insGlyPro | |
| ENST00000699999.1:n.249_254dup | ||
| ENST00000700000.1:c.165_170dup | ENSP00000514749.1:p.Pro57_Arg58insGlyPro | |
| ENST00000700001.1:n.237_242dup | ||
| ENST00000700002.1:c.165_170dup | ENSP00000514750.1:p.Pro57_Arg58insGlyPro | |
| ENST00000700003.1:c.165_170dup | ENSP00000514751.1:p.Pro57_Arg58insGlyPro | |
| ENST00000234420.11:c.165_170dup MANE Select | ENSP00000234420.5:p.Pro57_Arg58insGlyPro | |
| ENST00000540021.6:c.165_170dup | ENSP00000446475.1:p.Pro57_Arg58insGlyPro | |
| ENST00000652107.1:c.-37-7529_-37-7524dup | ENSP00000498629.1:n.-37-7529_-37-7524dup | |
| ENST00000673637.1:c.-38+167_-38+172dup | ENSP00000501310.1:n.-38+167_-38+172dup | |
| ENST00000673922.1:n.254_259dup | ||
| ENST00000234420.9:c.165_170dup | ENSP00000234420.4:p.Pro57_Arg58insGlyPro | |
| ENST00000445503.5:c.165_170dup | ENSP00000405294.1:p.Pro57_Arg58insGlyPro | |
| ENST00000456246.1:c.165_170dup | ENSP00000410570.1:p.Pro57_Arg58insGlyPro | |
| ENST00000493177.1:n.229_234dup | ||
| ENST00000540021.5:c.165_170dup | ENSP00000446475.1:p.Pro57_Arg58insGlyPro | |
| ENST00000606499.1:c.-37-7529_-37-7524dup | ENSP00000475605.1:n.-37-7529_-37-7524dup | |
| ENST00000614496.4:c.-572_-567dup | ENSP00000477844.1:n.-572_-567dup | |
| ENST00000616033.4:c.163_168dup | ENSP00000480261.1:p.Ala56_Arg57insTrpAla | |
| ENST00000622629.4:c.-2932_-2927dup | ENSP00000482078.1:n.-2932_-2927dup | |
| NM_000179.2:c.165_170dup , LRG_219t1:c.165_170dup | NP_000170.1:p.Pro57_Arg58insGlyPro | |
| NM_001281492.1:c.165_170dup | NP_001268421.1:p.Pro57_Arg58insGlyPro | |
| NM_001281493.1:c.-572_-567dup | NP_001268422.1:n.-572_-567dup | |
| XM_011532800.1:c.-38+167_-38+172dup | XP_011531102.1:n.-38+167_-38+172dup | |
| XM_024452819.1:c.165_170dup | XP_024308587.1:p.Pro57_Arg58insGlyPro | |
| XM_024452822.1:c.-572_-567dup | XP_024308590.1:n.-572_-567dup | |
| NM_000179.3:c.165_170dup MANE Select | NP_000170.1:p.Pro57_Arg58insGlyPro | |
| NM_001281492.2:c.165_170dup | NP_001268421.1:p.Pro57_Arg58insGlyPro | |
| NM_001281493.2:c.-572_-567dup | NP_001268422.1:n.-572_-567dup |