Linked Data
ClinVar Variation Id:
214792
dbSNP Id:
rs375650413
ExAC:
1:161176206 C / T
gnomAD v2:
1-161176206-C-T
gnomAD v3:
1-161206416-C-T
gnomAD v4:
1-161206416-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161206416C>T , CM000663.2:g.161206416C>T | GRCh38 |
| NC_000001.10:g.161176206C>T , CM000663.1:g.161176206C>T | GRCh37 |
| NC_000001.9:g.159442830C>T | NCBI36 |
| NG_013352.1:g.12102C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392179.5:c.212C>T | ENSP00000376018.4:p.Pro71Leu | |
| ENST00000467295.6:n.740C>T | ||
| ENST00000480762.6:n.126C>T | ||
| ENST00000493849.6:n.311C>T | ||
| ENST00000496553.6:n.951C>T | ||
| ENST00000676535.1:n.515C>T | ||
| ENST00000676583.1:c.212C>T | ENSP00000503681.1:p.Pro71Leu | |
| ENST00000676600.1:c.212C>T | ENSP00000503989.1:p.Pro71Leu | |
| ENST00000676653.1:n.528C>T | ||
| ENST00000676726.1:n.311C>T | ||
| ENST00000676770.1:n.1078C>T | ||
| ENST00000676795.1:c.96-2777C>T | ENSP00000504650.1:n.96-2777C>T | |
| ENST00000676871.1:n.311C>T | ||
| ENST00000676972.1:c.212C>T MANE Select | ENSP00000503117.1:p.Pro71Leu | |
| ENST00000676991.1:n.932C>T | ||
| ENST00000677033.1:n.1020C>T | ||
| ENST00000677045.1:c.105C>T | ENSP00000504168.1:p.Pro35= | |
| ENST00000677050.1:n.311C>T | ||
| ENST00000677063.1:c.105C>T | ENSP00000504572.1:p.Pro35= | |
| ENST00000677081.1:c.212C>T | ENSP00000503728.1:p.Pro71Leu | |
| ENST00000677089.1:n.126C>T | ||
| ENST00000677103.1:n.103-2777C>T | ||
| ENST00000677138.1:c.212C>T | ENSP00000504839.1:p.Pro71Leu | |
| ENST00000677178.1:n.515C>T | ||
| ENST00000677231.1:c.212C>T | ENSP00000503378.1:p.Pro71Leu | |
| ENST00000677336.1:n.126C>T | ||
| ENST00000677350.1:n.515C>T | ||
| ENST00000677358.1:n.126C>T | ||
| ENST00000677383.1:n.515C>T | ||
| ENST00000677453.1:c.212C>T | ENSP00000503604.1:p.Pro71Leu | |
| ENST00000677457.1:c.212C>T | ENSP00000503294.1:p.Pro71Leu | |
| ENST00000677471.1:n.126C>T | ||
| ENST00000677495.1:n.311C>T | ||
| ENST00000677547.1:c.212C>T | ENSP00000504269.1:p.Pro71Leu | |
| ENST00000677550.1:c.212C>T | ENSP00000503353.1:p.Pro71Leu | |
| ENST00000677577.1:n.311C>T | ||
| ENST00000677579.1:c.212C>T | ENSP00000504162.1:p.Pro71Leu | |
| ENST00000677613.1:c.212C>T | ENSP00000504258.1:p.Pro71Leu | |
| ENST00000677643.1:n.126C>T | ||
| ENST00000677653.1:c.212C>T | ENSP00000504542.1:p.Pro71Leu | |
| ENST00000677657.1:n.311C>T | ||
| ENST00000677736.1:n.311C>T | ||
| ENST00000677745.1:n.126C>T | ||
| ENST00000677807.1:n.515C>T | ||
| ENST00000677809.1:n.515C>T | ||
| ENST00000677837.1:c.105C>T | ENSP00000503661.1:p.Pro35= | |
| ENST00000677846.1:c.212C>T | ENSP00000504065.1:p.Pro71Leu | |
| ENST00000677916.1:n.311C>T | ||
| ENST00000677925.1:n.515C>T | ||
| ENST00000677948.1:c.105C>T | ENSP00000503510.1:p.Pro35= | |
| ENST00000678052.1:n.515C>T | ||
| ENST00000678068.1:n.1187C>T | ||
| ENST00000678130.1:n.923C>T | ||
| ENST00000678328.1:n.311C>T | ||
| ENST00000678356.1:n.632C>T | ||
| ENST00000678484.1:n.311C>T | ||
| ENST00000678492.1:n.515C>T | ||
| ENST00000678507.1:c.212C>T | ENSP00000504199.1:p.Pro71Leu | |
| ENST00000678511.1:c.212C>T | ENSP00000504846.1:p.Pro71Leu | |
| ENST00000678532.1:c.105C>T | ENSP00000504682.1:p.Pro35= | |
| ENST00000678559.1:c.105C>T | ENSP00000504285.1:p.Pro35= | |
| ENST00000678605.1:c.212C>T | ENSP00000503969.1:p.Pro71Leu | |
| ENST00000678613.1:n.515C>T | ||
| ENST00000678648.1:n.126C>T | ||
| ENST00000678783.1:c.212C>T | ENSP00000504215.1:p.Pro71Leu | |
| ENST00000678793.1:c.212C>T | ENSP00000503431.1:p.Pro71Leu | |
| ENST00000678850.1:n.311C>T | ||
| ENST00000678880.1:c.105C>T | ENSP00000503015.1:p.Pro35= | |
| ENST00000678911.1:c.212C>T | ENSP00000503946.1:p.Pro71Leu | |
| ENST00000678966.1:n.515C>T | ||
| ENST00000678982.1:c.105C>T | ENSP00000504597.1:p.Pro35= | |
| ENST00000679064.1:c.212C>T | ENSP00000502868.1:p.Pro71Leu | |
| ENST00000679071.1:n.304C>T | ||
| ENST00000679142.1:c.189C>T | ENSP00000504800.1:n.189C>T | |
| ENST00000679169.1:c.105C>T | ENSP00000504096.1:p.Pro35= | |
| ENST00000679176.1:c.212C>T | ENSP00000504170.1:p.Pro71Leu | |
| ENST00000679215.1:n.515C>T | ||
| ENST00000679218.1:c.263C>T | ENSP00000504577.1:p.Pro88Leu | |
| ENST00000679239.1:c.212C>T | ENSP00000504555.1:p.Pro71Leu | |
| ENST00000679282.1:c.212C>T | ENSP00000504533.1:p.Pro71Leu | |
| ENST00000367993.7:c.212C>T | ENSP00000356972.3:p.Pro71Leu | |
| ENST00000392179.4:c.212C>T | ENSP00000376018.4:p.Pro71Leu | |
| ENST00000467295.5:n.300C>T | ||
| ENST00000473321.1:n.8C>T | ||
| ENST00000478866.5:n.222C>T | ||
| ENST00000479948.5:n.504C>T | ||
| ENST00000496133.5:n.520C>T | ||
| ENST00000496553.5:n.552C>T | ||
| NM_001166159.1:c.212C>T | NP_001159631.1:p.Pro71Leu | |
| NM_004550.4:c.212C>T | NP_004541.1:p.Pro71Leu | |
| XM_005245208.1:c.212C>T | XP_005245265.1:p.Pro71Leu | |
| XM_005245209.1:c.-83C>T | XP_005245266.1:n.-83C>T | |
| XM_005245209.2:c.-83C>T | XP_005245266.1:n.-83C>T | |
| NM_001166159.2:c.212C>T | NP_001159631.1:p.Pro71Leu | |
| NM_001377298.1:c.212C>T | NP_001364227.1:p.Pro71Leu | |
| NM_001377299.1:c.212C>T MANE Select | NP_001364228.1:p.Pro71Leu | |
| NM_001377300.1:c.212C>T | NP_001364229.1:p.Pro71Leu | |
| NM_001377301.1:c.212C>T | NP_001364230.1:p.Pro71Leu | |
| NM_001377302.1:c.212C>T | NP_001364231.1:p.Pro71Leu | |
| NR_165188.1:n.231C>T | ||
| NM_004550.5:c.212C>T | NP_004541.1:p.Pro71Leu |