Linked Data
ClinVar Variation Id:
2122286
ClinVar RCV Id:
RCV003053974
gnomAD v4:
3-15645042-T-TCTGAGATGATGTATGACAATTTCACC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.15645046_15645071dup , CM000665.2:g.15645046_15645071dup | GRCh38 |
| NC_000003.11:g.15686553_15686578dup , CM000665.1:g.15686553_15686578dup | GRCh37 |
| NC_000003.10:g.15661557_15661582dup | NCBI36 |
| NG_008019.1:g.48299_48324dup | |
| NG_008019.2:g.48695_48720dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436193.6:c.1130_1155dup | ENSP00000394277.2:p.Val386ArgfsTer2 | |
| ENST00000671928.2:c.399+2989_399+3014dup | ENSP00000500069.2:n.399+2989_399+3014dup | |
| ENST00000672892.2:c.1015+115_1015+140dup | ENSP00000499944.2:n.1015+115_1015+140dup | |
| ENST00000303498.10:c.1130_1155dup | ENSP00000306477.6:p.Val386ArgfsTer2 | |
| ENST00000427382.2:c.1130_1155dup | ENSP00000397113.2:p.Val386ArgfsTer2 | |
| ENST00000437172.6:c.1130_1155dup | ENSP00000400995.2:p.Val386ArgfsTer2 | |
| ENST00000449107.7:c.1130_1155dup | ENSP00000388212.2:p.Val386ArgfsTer2 | |
| ENST00000643237.3:c.1130_1155dup MANE Select | ENSP00000495254.2:p.Val386ArgfsTer2 | |
| ENST00000646371.1:c.1130_1155dup | ENSP00000495866.1:p.Val386ArgfsTer2 | |
| ENST00000671928.1:c.165+2989_165+3014dup | ENSP00000500069.1:n.165+2989_165+3014dup | |
| ENST00000672065.1:c.1190_1215dup | ENSP00000500403.1:p.Val406ArgfsTer2 | |
| ENST00000672112.1:c.1196_1221dup | ENSP00000500193.1:p.Val408ArgfsTer2 | |
| ENST00000672141.1:c.399+2989_399+3014dup | ENSP00000500210.1:n.399+2989_399+3014dup | |
| ENST00000672427.1:c.1015+115_1015+140dup | ENSP00000500131.1:n.1015+115_1015+140dup | |
| ENST00000672760.1:c.399+2989_399+3014dup | ENSP00000500530.1:n.399+2989_399+3014dup | |
| ENST00000672892.1:c.793+115_793+140dup | ENSP00000499944.1:n.793+115_793+140dup | |
| ENST00000673467.1:c.399+2989_399+3014dup | ENSP00000500288.1:n.399+2989_399+3014dup | |
| ENST00000673620.1:c.399+2989_399+3014dup | ENSP00000500325.1:n.399+2989_399+3014dup | |
| ENST00000303498.9:c.1190_1215dup | ENSP00000306477.5:p.Val406ArgfsTer2 | |
| ENST00000383778.5:c.1130_1155dup | ENSP00000373288.4:p.Val386ArgfsTer2 | |
| ENST00000437172.5:c.1196_1221dup | ENSP00000400995.1:p.Val408ArgfsTer2 | |
| ENST00000449107.5:c.1196_1221dup | ENSP00000388212.1:p.Val408ArgfsTer2 | |
| NM_000060.3:c.1190_1215dup | NP_000051.1:p.Val406ArgfsTer2 | |
| NM_001281723.1:c.1196_1221dup | NP_001268652.1:p.Val408ArgfsTer2 | |
| NM_001281724.1:c.1196_1221dup | NP_001268653.1:p.Val408ArgfsTer2 | |
| NM_001281725.1:c.1130_1155dup | NP_001268654.1:p.Val386ArgfsTer2 | |
| XM_006713314.2:c.1130_1155dup | XP_006713377.1:p.Val386ArgfsTer2 | |
| XM_011534041.1:c.1130_1155dup | XP_011532343.1:p.Val386ArgfsTer2 | |
| NM_000060.4:c.1190_1215dup | NP_000051.1:p.Val406ArgfsTer2 | |
| NM_001281723.2:c.1196_1221dup | NP_001268652.1:p.Val408ArgfsTer2 | |
| NM_001281724.2:c.1196_1221dup | NP_001268653.1:p.Val408ArgfsTer2 | |
| NM_001281725.2:c.1130_1155dup | NP_001268654.1:p.Val386ArgfsTer2 | |
| NM_001323582.1:c.1130_1155dup | NP_001310511.1:p.Val386ArgfsTer2 | |
| XM_011534041.2:c.1130_1155dup | XP_011532343.1:p.Val386ArgfsTer2 | |
| XM_017007088.1:c.1130_1155dup | XP_016862577.1:p.Val386ArgfsTer2 | |
| XM_024453724.1:c.1130_1155dup | XP_024309492.1:p.Val386ArgfsTer2 | |
| NM_001281723.3:c.1130_1155dup | NP_001268652.2:p.Val386ArgfsTer2 | |
| NM_001281724.3:c.1130_1155dup | NP_001268653.2:p.Val386ArgfsTer2 | |
| NM_001370658.1:c.1130_1155dup MANE Select | NP_001357587.1:p.Val386ArgfsTer2 | |
| NM_001370752.1:c.1015+115_1015+140dup | NP_001357681.1:n.1015+115_1015+140dup | |
| NM_001370753.1:c.399+2989_399+3014dup | NP_001357682.1:n.399+2989_399+3014dup | |
| NM_001281726.2:c.*2908_*2933dup | NP_001268655.2:n.*2908_*2933dup |