Linked Data
dbSNP Id:
rs1855341232
gnomAD v3:
11-6610045-G-A
gnomAD v4:
11-6610045-G-A
MyVariant Identifiers:
chr11:g.6631276G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6610045G>A , CM000673.2:g.6610045G>A | GRCh38 |
| NC_000011.9:g.6631276G>A , CM000673.1:g.6631276G>A | GRCh37 |
| NC_000011.8:g.6587852G>A | NCBI36 |
| NG_029702.1:g.11313G>A , LRG_444:g.11313G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299421.9:c.1078+10G>A (ILK) MANE Select | ENSP00000299421.4:n.1078+10G>A | |
| ENST00000299424.9:c.*877C>T (TAF10) MANE Select | ENSP00000299424.4:n.*877C>T | |
| ENST00000299421.8:c.1078+10G>A (ILK) | ENSP00000299421.3:n.1078+10G>A | |
| ENST00000396751.6:c.1078+10G>A (ILK) | ENSP00000379975.2:n.1078+10G>A | |
| ENST00000420936.6:c.1078+10G>A (ILK) | ENSP00000403487.2:n.1078+10G>A | |
| ENST00000526318.2:c.328-558G>A (ILK) | ENSP00000480597.1:n.328-558G>A | |
| ENST00000526711.5:c.*789+10G>A (ILK) | ENSP00000479932.1:n.*789+10G>A | |
| ENST00000528995.5:c.895+10G>A (ILK) | ENSP00000435323.1:n.895+10G>A | |
| ENST00000530016.5:n.1415+10G>A (ILK) | ||
| ENST00000532063.5:c.676+10G>A (ILK) | ENSP00000434492.2:n.676+10G>A | |
| ENST00000537806.5:c.1171+10G>A (ILK) | ENSP00000439606.2:n.1171+10G>A | |
| ENST00000616342.1:n.1643C>T (TAF10) | ||
| NM_001014794.2:c.1078+10G>A (ILK) | NP_001014794.1:n.1078+10G>A | |
| NM_001014795.2:c.1078+10G>A (ILK) | NP_001014795.1:n.1078+10G>A | |
| NM_001278441.1:c.895+10G>A (ILK) | NP_001265370.1:n.895+10G>A | |
| NM_001278442.1:c.676+10G>A (ILK) | NP_001265371.1:n.676+10G>A | |
| NM_004517.3:c.1078+10G>A (ILK) | NP_004508.1:n.1078+10G>A | |
| XM_005252904.3:c.1078+10G>A (ILK) | XP_005252961.1:n.1078+10G>A | |
| XM_005252905.1:c.676+10G>A (ILK) | XP_005252962.1:n.676+10G>A | |
| XM_011520065.1:c.1078+10G>A (ILK) | XP_011518367.1:n.1078+10G>A | |
| XM_005252904.5:c.1078+10G>A (ILK) | XP_005252961.1:n.1078+10G>A | |
| XM_005252905.3:c.676+10G>A (ILK) | XP_005252962.1:n.676+10G>A | |
| XM_017017672.1:c.925+10G>A (ILK) | XP_016873161.1:n.925+10G>A | |
| XM_024448494.1:c.1171+10G>A (ILK) | XP_024304262.1:n.1171+10G>A | |
| XM_024448495.1:c.1171+10G>A (ILK) | XP_024304263.1:n.1171+10G>A | |
| XM_024448496.1:c.1171+10G>A (ILK) | XP_024304264.1:n.1171+10G>A | |
| XM_024448497.1:c.1171+10G>A (ILK) | XP_024304265.1:n.1171+10G>A | |
| XM_024448498.1:c.925+10G>A (ILK) | XP_024304266.1:n.925+10G>A | |
| XM_024448499.1:c.925+10G>A (ILK) | XP_024304267.1:n.925+10G>A | |
| XM_024448500.1:c.769+10G>A (ILK) | XP_024304268.1:n.769+10G>A | |
| NM_006284.4:c.*877C>T (TAF10) MANE Select | NP_006275.1:n.*877C>T | |
| NM_001014794.3:c.1078+10G>A (ILK) | NP_001014794.1:n.1078+10G>A | |
| NM_001014795.3:c.1078+10G>A (ILK) | NP_001014795.1:n.1078+10G>A | |
| NM_001278441.2:c.895+10G>A (ILK) | NP_001265370.1:n.895+10G>A | |
| NM_004517.4:c.1078+10G>A (ILK) MANE Select | NP_004508.1:n.1078+10G>A | |
| NM_001278442.2:c.676+10G>A (ILK) | NP_001265371.1:n.676+10G>A |