Linked Data
ClinVar Variation Id:
1722328
ClinVar RCV Id:
RCV002302442
COSMIC:
COSM5812115
MyVariant Identifiers:
chr11:g.10051312C>T (hg19)
MutSpliceDB:
CA473081533
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.10029765C>T , CM000673.2:g.10029765C>T | GRCh38 |
| NC_000011.9:g.10051312C>T , CM000673.1:g.10051312C>T | GRCh37 |
| NC_000011.8:g.10007888C>T | NCBI36 |
| NG_008074.1:g.269443G>A , LRG_267:g.269443G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526353.2:n.663G>A | ||
| ENST00000527019.6:n.460G>A | ||
| ENST00000533661.2:n.469G>A | ||
| ENST00000533770.6:c.513G>A | ENSP00000509247.1:p.Gln171= | |
| ENST00000675281.2:c.513G>A | ENSP00000502491.1:p.Gln171= | |
| ENST00000676324.2:c.513G>A | ENSP00000502578.1:p.Gln171= | |
| ENST00000676387.2:c.513G>A | ENSP00000502779.1:p.Gln171= | |
| ENST00000685217.1:n.844G>A | ||
| ENST00000686079.1:c.513G>A | ENSP00000509599.1:p.Gln171= | |
| ENST00000687210.1:c.513G>A | ENSP00000509480.1:p.Gln171= | |
| ENST00000687256.1:c.513G>A | ENSP00000508741.1:p.Gln171= | |
| ENST00000687300.1:c.513G>A | ENSP00000508415.1:p.Gln171= | |
| ENST00000688206.1:c.513G>A | ENSP00000510516.1:p.Gln171= | |
| ENST00000688344.1:c.234G>A | ENSP00000509987.1:p.Gln78= | |
| ENST00000688417.1:n.663G>A | ||
| ENST00000689128.1:c.513G>A | ENSP00000509587.1:p.Gln171= | |
| ENST00000689258.1:c.375G>A | ENSP00000510475.1:p.Gln125= | |
| ENST00000689940.1:c.513G>A | ENSP00000508452.1:p.Gln171= | |
| ENST00000692716.1:c.513G>A | ENSP00000509545.1:p.Gln171= | |
| ENST00000693022.1:c.513G>A | ENSP00000508914.1:p.Gln171= | |
| ENST00000693201.1:c.*95G>A | ENSP00000510346.1:n.*95G>A | |
| ENST00000693212.1:c.513G>A | ENSP00000510716.1:p.Gln171= | |
| ENST00000256190.13:c.513G>A MANE Select | ENSP00000256190.8:p.Gln171= | |
| ENST00000675281.1:c.513G>A | ENSP00000502491.1:p.Gln171= | |
| ENST00000676324.1:c.513G>A | ENSP00000502578.1:p.Gln171= | |
| ENST00000676387.1:c.513G>A | ENSP00000502779.1:p.Gln171= | |
| ENST00000256190.12:c.513G>A | ENSP00000256190.8:p.Gln171= | |
| ENST00000527019.5:n.460G>A | ||
| ENST00000533661.1:n.381G>A | ||
| ENST00000533770.5:n.428G>A | ||
| ENST00000617179.4:c.372G>A | ENSP00000482806.1:p.Gln124= | |
| NM_030962.3:c.513G>A , LRG_267t1:c.513G>A | NP_112224.1:p.Gln171= | |
| XM_005253154.3:c.513G>A | XP_005253211.1:p.Gln171= | |
| XM_005253155.3:c.513G>A | XP_005253212.1:p.Gln171= | |
| XM_011520394.1:c.513G>A | XP_011518696.1:p.Gln171= | |
| XM_011520395.1:c.513G>A | XP_011518697.1:p.Gln171= | |
| XM_011520396.1:c.513G>A | XP_011518698.1:p.Gln171= | |
| XM_005253154.5:c.513G>A | XP_005253211.1:p.Gln171= | |
| XM_005253155.5:c.513G>A | XP_005253212.1:p.Gln171= | |
| XM_011520394.3:c.513G>A | XP_011518696.1:p.Gln171= | |
| XM_011520395.3:c.513G>A | XP_011518697.1:p.Gln171= | |
| XM_011520396.3:c.513G>A | XP_011518698.1:p.Gln171= | |
| XM_017018372.2:c.375G>A | XP_016873861.1:p.Gln125= | |
| XM_017018373.2:c.375G>A | XP_016873862.1:p.Gln125= | |
| XM_017018374.2:c.513G>A | XP_016873863.1:p.Gln171= | |
| XM_017018375.2:c.513G>A | XP_016873864.1:p.Gln171= | |
| XM_017018376.2:c.513G>A | XP_016873865.1:p.Gln171= | |
| XM_017018377.2:c.513G>A | XP_016873866.1:p.Gln171= | |
| XR_001747994.2:n.651G>A | ||
| NM_001386339.1:c.513G>A | NP_001373268.1:p.Gln171= | |
| NM_001386342.1:c.513G>A | NP_001373271.1:p.Gln171= | |
| NM_030962.4:c.513G>A MANE Select | NP_112224.1:p.Gln171= |