Linked Data
ClinVar Variation Id:
546377
ClinVar RCV Id:
RCV000658242
dbSNP Id:
rs1553179349
COSMIC:
COSM4413486
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11157263A>G , CM000663.2:g.11157263A>G | GRCh38 |
| NC_000001.10:g.11217320A>G , CM000663.1:g.11217320A>G | GRCh37 |
| NC_000001.9:g.11139907A>G | NCBI36 |
| NG_033239.1:g.110289T>C , LRG_734:g.110289T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703118.1:c.4358T>C | ENSP00000515181.1:p.Leu1453Pro | |
| ENST00000703131.1:n.278T>C | ||
| ENST00000703140.1:c.4145T>C | ENSP00000515197.1:p.Leu1382Pro | |
| ENST00000703141.1:c.4358T>C | ENSP00000515198.1:p.Leu1453Pro | |
| ENST00000703142.1:c.*1188T>C | ENSP00000515199.1:n.*1188T>C | |
| ENST00000361445.9:c.4358T>C MANE Select | ENSP00000354558.4:p.Leu1453Pro | |
| ENST00000361445.8:c.4358T>C | ENSP00000354558.4:p.Leu1453Pro | |
| NM_004958.3:c.4358T>C , LRG_734t1:c.4358T>C | NP_004949.1:p.Leu1453Pro | |
| XM_005263438.1:c.4358T>C | XP_005263495.1:p.Leu1453Pro | |
| XM_011541166.1:c.4358T>C | XP_011539468.1:p.Leu1453Pro | |
| XR_244786.1:n.4479T>C | ||
| XM_005263438.2:c.4358T>C | XP_005263495.1:p.Leu1453Pro | |
| XM_011541166.2:c.4358T>C | XP_011539468.1:p.Leu1453Pro | |
| XM_017000900.1:c.3677T>C | XP_016856389.1:p.Leu1226Pro | |
| XM_017000901.1:c.3110T>C | XP_016856390.1:p.Leu1037Pro | |
| XM_024446187.1:c.4358T>C | XP_024301955.1:p.Leu1453Pro | |
| XR_001737087.1:n.4479T>C | ||
| NM_004958.4:c.4358T>C MANE Select | NP_004949.1:p.Leu1453Pro | |
| NM_001386500.1:c.4358T>C | NP_001373429.1:p.Leu1453Pro | |
| NM_001386501.1:c.3110T>C | NP_001373430.1:p.Leu1037Pro |