Linked Data
ClinVar Variation Id:
1541585
ClinVar RCV Id:
RCV002164655
dbSNP Id:
rs1381722107
MyVariant Identifiers:
chr11:g.71146531G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435485G>A , CM000673.2:g.71435485G>A | GRCh38 |
| NC_000011.9:g.71146531G>A , CM000673.1:g.71146531G>A | GRCh37 |
| NC_000011.8:g.70824179G>A | NCBI36 |
| NG_012655.2:g.17947C>T , LRG_340:g.17947C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1318C>T | ENSP00000435707.3:p.Leu440= | |
| ENST00000526780.6:c.1318C>T | ENSP00000435668.2:p.Leu440= | |
| ENST00000527316.6:c.1144C>T | ENSP00000435047.2:p.Leu382= | |
| ENST00000682708.1:c.1369C>T | ENSP00000506866.1:p.Leu457= | |
| ENST00000683287.1:c.1354C>T | ENSP00000507607.1:p.Leu452= | |
| ENST00000683714.1:c.*81C>T | ENSP00000508207.1:n.*81C>T | |
| ENST00000684396.1:n.1358C>T | ||
| ENST00000685320.1:c.733C>T | ENSP00000509319.1:p.Leu245= | |
| ENST00000690257.1:c.1222C>T | ENSP00000510750.1:p.Leu408= | |
| ENST00000355527.8:c.1318C>T MANE Select | ENSP00000347717.4:p.Leu440= | |
| ENST00000355527.7:c.1318C>T | ENSP00000347717.3:p.Leu440= | |
| ENST00000407721.6:c.1318C>T | ENSP00000384739.2:p.Leu440= | |
| ENST00000525137.1:c.819C>T | ENSP00000435956.1:n.819C>T | |
| ENST00000533800.5:c.568C>T | ENSP00000435011.1:p.Leu190= | |
| ENST00000534795.5:c.319+2327C>T | ||
| NM_001163817.1:c.1318C>T | NP_001157289.1:p.Leu440= | |
| NM_001360.2:c.1318C>T , LRG_340t1:c.1318C>T | NP_001351.2:p.Leu440= | |
| XM_011544777.1:c.*81C>T | XP_011543079.1:n.*81C>T | |
| XM_011544777.2:c.*81C>T | XP_011543079.1:n.*81C>T | |
| NM_001163817.2:c.1318C>T | NP_001157289.1:p.Leu440= | |
| NM_001360.3:c.1318C>T MANE Select | NP_001351.2:p.Leu440= |