Linked Data
ClinVar Variation Id:
189715
ClinVar RCV Id:
RCV000170210
dbSNP Id:
rs1557135125
PubMed:
PMID:16473305
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154030559_154031117del , CM000685.2:g.154030559_154031117del | GRCh38 |
| NC_000023.10:g.153296010_153296568del , CM000685.1:g.153296010_153296568del | GRCh37 |
| NC_000023.9:g.152949204_152949762del | NCBI36 |
| NG_007107.2:g.111011_111569del | |
| NG_007107.3:g.110987_111545del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303391.11:c.711_1269del MANE Plus Clinical | ENSP00000301948.6:p.Gly238TrpfsTer? | |
| ENST00000453960.7:c.747_1305del MANE Select | ENSP00000395535.2:p.Gly250TrpfsTer? | |
| ENST00000303391.10:c.711_1269del | ENSP00000301948.6:p.Gly238TrpfsTer? | |
| ENST00000453960.6:c.747_1305del | ENSP00000395535.2:p.Gly250TrpfsTer? | |
| ENST00000619732.4:c.711_1269del | ENSP00000480973.1:p.Gly238TrpfsTer? | |
| ENST00000628176.2:c.*83_*641del | ENSP00000486978.1:n.*83_*641del | |
| NM_001110792.1:c.747_1305del | NP_001104262.1:p.Gly250TrpfsTer? | |
| NM_001316337.1:c.432_990del | NP_001303266.1:p.Gly145TrpfsTer? | |
| NM_004992.3:c.711_1269del | NP_004983.1:p.Gly238TrpfsTer? | |
| XM_005274681.3:c.711_1269del | XP_005274738.1:p.Gly238TrpfsTer? | |
| XM_005274682.3:c.432_990del | XP_005274739.1:p.Gly145TrpfsTer? | |
| XM_005274683.3:c.432_990del | XP_005274740.1:p.Gly145TrpfsTer? | |
| XM_006724819.2:c.42_600del | XP_006724882.1:p.Gly15TrpfsTer? | |
| XM_011531166.1:c.432_990del | XP_011529468.1:p.Gly145TrpfsTer? | |
| XM_006724819.3:c.42_600del | XP_006724882.1:p.Gly15TrpfsTer? | |
| XM_011531166.2:c.432_990del | XP_011529468.1:p.Gly145TrpfsTer? | |
| XM_024452383.1:c.432_990del | XP_024308151.1:p.Gly145TrpfsTer? | |
| XM_024452384.1:c.432_990del | XP_024308152.1:p.Gly145TrpfsTer? | |
| NM_001110792.2:c.747_1305del MANE Select | NP_001104262.1:p.Gly250TrpfsTer? | |
| NM_001316337.2:c.432_990del | NP_001303266.1:p.Gly145TrpfsTer? | |
| NM_001369391.2:c.432_990del | NP_001356320.1:p.Gly145TrpfsTer? | |
| NM_001369392.2:c.432_990del | NP_001356321.1:p.Gly145TrpfsTer? | |
| NM_001369393.2:c.432_990del | NP_001356322.1:p.Gly145TrpfsTer? | |
| NM_001369394.1:c.432_990del | NP_001356323.1:p.Gly145TrpfsTer? | |
| NM_001369394.2:c.432_990del | NP_001356323.1:p.Gly145TrpfsTer? | |
| NM_001386137.1:c.42_600del | NP_001373066.1:p.Gly15TrpfsTer? | |
| NM_001386138.1:c.42_600del | NP_001373067.1:p.Gly15TrpfsTer? | |
| NM_001386139.1:c.42_600del | NP_001373068.1:p.Gly15TrpfsTer? | |
| NM_004992.4:c.711_1269del MANE Plus Clinical | NP_004983.1:p.Gly238TrpfsTer? |