Linked Data
ClinVar Variation Id:
143614
ClinVar RCV Id:
RCV000133154
dbSNP Id:
rs61749703
PubMed:
PMID:12075485
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154031299del , CM000685.2:g.154031299del | GRCh38 |
| NC_000023.10:g.153296750del , CM000685.1:g.153296750del | GRCh37 |
| NC_000023.9:g.152949944del | NCBI36 |
| NG_007107.2:g.110831del | |
| NG_007107.3:g.110807del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.531del MANE Plus Clinical | ENSP00000301948.6:p.Lys177AsnfsTer? | |
| ENST00000453960.7:c.567del MANE Select | ENSP00000395535.2:p.Lys189AsnfsTer? | |
| ENST00000637917.1:c.65+99del | ||
| ENST00000303391.10:c.531del | ENSP00000301948.6:p.Lys177AsnfsTer? | |
| ENST00000407218.5:c.469-11del | ENSP00000384865.2:n.469-11del | |
| ENST00000453960.6:c.567del | ENSP00000395535.2:p.Lys189AsnfsTer? | |
| ENST00000486506.5:n.2879del | ||
| ENST00000619732.4:c.531del | ENSP00000480973.1:p.Lys177AsnfsTer? | |
| ENST00000622433.4:c.519del | ENSP00000484470.1:p.Lys173AsnfsTer? | |
| ENST00000628176.2:c.433-11del | ENSP00000486978.1:n.433-11del | |
| NM_001110792.1:c.567del | NP_001104262.1:p.Lys189AsnfsTer? | |
| NM_001316337.1:c.252del | NP_001303266.1:p.Lys84AsnfsTer? | |
| NM_004992.3:c.531del | NP_004983.1:p.Lys177AsnfsTer? | |
| XM_005274681.3:c.531del | XP_005274738.1:p.Lys177AsnfsTer? | |
| XM_005274682.3:c.252del | XP_005274739.1:p.Lys84AsnfsTer? | |
| XM_005274683.3:c.252del | XP_005274740.1:p.Lys84AsnfsTer? | |
| XM_006724819.2:c.-128-11del | XP_006724882.1:n.-128-11del | |
| XM_011531166.1:c.252del | XP_011529468.1:p.Lys84AsnfsTer? | |
| XM_006724819.3:c.-128-11del | XP_006724882.1:n.-128-11del | |
| XM_011531166.2:c.252del | XP_011529468.1:p.Lys84AsnfsTer? | |
| XM_024452383.1:c.252del | XP_024308151.1:p.Lys84AsnfsTer? | |
| XM_024452384.1:c.252del | XP_024308152.1:p.Lys84AsnfsTer? | |
| NM_001110792.2:c.567del MANE Select | NP_001104262.1:p.Lys189AsnfsTer? | |
| NM_001316337.2:c.252del | NP_001303266.1:p.Lys84AsnfsTer? | |
| NM_001369391.2:c.252del | NP_001356320.1:p.Lys84AsnfsTer? | |
| NM_001369392.2:c.252del | NP_001356321.1:p.Lys84AsnfsTer? | |
| NM_001369393.2:c.252del | NP_001356322.1:p.Lys84AsnfsTer? | |
| NM_001369394.1:c.252del | NP_001356323.1:p.Lys84AsnfsTer? | |
| NM_001369394.2:c.252del | NP_001356323.1:p.Lys84AsnfsTer? | |
| NM_001386137.1:c.-128-11del | NP_001373066.1:n.-128-11del | |
| NM_001386138.1:c.-128-11del | NP_001373067.1:n.-128-11del | |
| NM_001386139.1:c.-128-11del | NP_001373068.1:n.-128-11del | |
| NM_004992.4:c.531del MANE Plus Clinical | NP_004983.1:p.Lys177AsnfsTer? |