Linked Data
ClinVar Variation Id:
7550
ClinVar RCV Id:
RCV000007986
dbSNP Id:
rs121909149
PubMed:
PMID:11381256
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.2831573G>C , CM000666.2:g.2831573G>C | GRCh38 |
| NC_000004.11:g.2833300G>C , CM000666.1:g.2833300G>C | GRCh37 |
| NC_000004.10:g.2803098G>C | NCBI36 |
| NG_011609.1:g.43551G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435136.8:c.1328G>C | ENSP00000403231.3:p.Arg443Pro | |
| ENST00000503393.8:c.1244G>C MANE Select | ENSP00000422168.3:p.Arg415Pro | |
| ENST00000511747.6:c.1415G>C | ENSP00000424846.2:p.Arg472Pro | |
| ENST00000356331.9:c.1244G>C | ENSP00000348685.5:p.Arg415Pro | |
| ENST00000435136.6:c.1244G>C | ENSP00000403231.2:p.Arg415Pro | |
| ENST00000442312.6:c.1328G>C | ENSP00000388152.2:p.Arg443Pro | |
| ENST00000452765.6:c.1244G>C | ENSP00000409746.2:p.Arg415Pro | |
| ENST00000503393.6:c.1415G>C | ENSP00000422168.2:p.Arg472Pro | |
| ENST00000504450.1:n.541G>C | ||
| ENST00000510204.5:n.1721G>C | ||
| ENST00000511747.5:c.1244G>C | ENSP00000424846.1:p.Arg415Pro | |
| ENST00000513069.1:c.354G>C | ||
| ENST00000515737.5:c.*1129G>C | ENSP00000422605.1:n.*1129G>C | |
| ENST00000515802.5:n.1350G>C | ||
| NM_001122681.1:c.1244G>C | NP_001116153.1:p.Arg415Pro | |
| NM_001145855.1:c.1328G>C | NP_001139327.1:p.Arg443Pro | |
| NM_001145856.1:c.1415G>C | NP_001139328.1:p.Arg472Pro | |
| NM_003023.4:c.1244G>C | NP_003014.3:p.Arg415Pro | |
| XM_005247998.3:c.1253G>C | XP_005248055.1:p.Arg418Pro | |
| XM_005247999.3:c.1244G>C | XP_005248056.1:p.Arg415Pro | |
| XM_011513547.1:c.1415G>C | XP_011511849.1:p.Arg472Pro | |
| XM_011513548.1:c.1244G>C | XP_011511850.1:p.Arg415Pro | |
| XM_011513549.1:c.1244G>C | XP_011511851.1:p.Arg415Pro | |
| XM_011513550.1:c.1244G>C | XP_011511852.1:p.Arg415Pro | |
| XM_011513551.1:c.1244G>C | XP_011511853.1:p.Arg415Pro | |
| XM_011513552.1:c.1073G>C | XP_011511854.1:p.Arg358Pro | |
| XM_011513553.1:c.881G>C | XP_011511855.1:p.Arg294Pro | |
| XM_011513554.1:c.589G>C | XP_011511856.1:p.Asp197His | |
| XM_011513555.1:c.589G>C | XP_011511857.1:p.Asp197His | |
| XM_011513556.1:c.589G>C | XP_011511858.1:p.Asp197His | |
| XR_924990.1:n.1248G>C | ||
| NM_001122681.2:c.1244G>C MANE Select | NP_001116153.1:p.Arg415Pro | |
| NM_001145855.2:c.1328G>C | NP_001139327.1:p.Arg443Pro | |
| NM_001145856.2:c.1415G>C | NP_001139328.1:p.Arg472Pro |