Linked Data
ClinVar Variation Id:
8698
ClinVar RCV Id:
RCV003324490
dbSNP Id:
rs28936676
PubMed:
PMID:9811936
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161170467A>C , CM000663.2:g.161170467A>C | GRCh38 |
| NC_000001.10:g.161140257A>C , CM000663.1:g.161140257A>C | GRCh37 |
| NC_000001.9:g.159406881A>C | NCBI36 |
| NG_011480.1:g.12058T>G | |
| NG_012877.1:g.9077A>C | |
| NG_012877.2:g.9077A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367999.9:c.1046A>C MANE Select | ENSP00000356978.4:p.Asp349Ala | |
| ENST00000650741.1:c.841A>C | ENSP00000499106.1:n.841A>C | |
| ENST00000651150.1:c.*803A>C | ENSP00000498615.1:n.*803A>C | |
| ENST00000652100.1:c.107A>C | ||
| ENST00000652103.1:c.750A>C | ||
| ENST00000652182.1:c.988-153A>C | ENSP00000498884.1:n.988-153A>C | |
| ENST00000652297.1:c.802A>C | ENSP00000498871.1:n.802A>C | |
| ENST00000652473.1:c.*588A>C | ENSP00000498477.1:n.*588A>C | |
| ENST00000352210.9:c.1046A>C | ENSP00000343943.5:p.Asp349Ala | |
| ENST00000367999.8:c.1046A>C | ENSP00000356978.4:p.Asp349Ala | |
| ENST00000462866.5:n.96-153A>C | ||
| ENST00000466452.1:n.207A>C | ||
| ENST00000495483.5:n.1104A>C | ||
| ENST00000497522.5:n.474-153A>C | ||
| ENST00000535223.5:c.88-153A>C | ENSP00000443769.1:n.88-153A>C | |
| ENST00000537523.5:c.304A>C | ||
| ENST00000537829.1:c.214A>C | ||
| ENST00000539753.5:c.342A>C | ENSP00000439613.1:p.Ter114Cys | |
| ENST00000541818.1:n.800A>C | ||
| ENST00000544598.5:c.223-153A>C | ENSP00000444216.1:n.223-153A>C | |
| NM_000309.3:c.1046A>C | NP_000300.1:p.Asp349Ala | |
| NM_001122764.1:c.1046A>C | NP_001116236.1:p.Asp349Ala | |
| XM_005245291.3:c.1046A>C | XP_005245348.2:p.Asp349Ala | |
| XM_005245295.3:c.638A>C | XP_005245352.2:p.Asp213Ala | |
| XM_006711402.2:c.1061A>C | XP_006711465.2:p.Asp354Ala | |
| XM_006711403.2:c.1046A>C | XP_006711466.2:p.Asp349Ala | |
| XM_006711404.2:c.1061A>C | XP_006711467.1:p.Asp354Ala | |
| XM_006711406.2:c.638A>C | XP_006711469.2:p.Asp213Ala | |
| XM_011509663.1:c.1175A>C | XP_011507965.1:p.Asp392Ala | |
| XM_011509664.1:c.1160A>C | XP_011507966.1:p.Asp387Ala | |
| XM_011509665.1:c.1175A>C | XP_011507967.1:p.Asp392Ala | |
| XM_011509666.1:c.1117-153A>C | XP_011507968.1:n.1117-153A>C | |
| XM_011509667.1:c.1061A>C | XP_011507969.1:p.Asp354Ala | |
| XM_011509668.1:c.1061A>C | XP_011507970.1:p.Asp354Ala | |
| XM_011509669.1:c.1061A>C | XP_011507971.1:p.Asp354Ala | |
| XM_011509670.1:c.1061A>C | XP_011507972.1:p.Asp354Ala | |
| XM_011509671.1:c.1160A>C | XP_011507973.1:p.Asp387Ala | |
| XM_011509672.1:c.1061A>C | XP_011507974.1:p.Asp354Ala | |
| XM_011509673.1:c.911A>C | XP_011507975.1:p.Asp304Ala | |
| XM_011509674.1:c.937-153A>C | XP_011507976.1:n.937-153A>C | |
| XM_011509675.1:c.947A>C | XP_011507977.1:p.Asp316Ala | |
| XM_011509676.1:c.638A>C | XP_011507978.1:p.Asp213Ala | |
| XM_011509677.1:c.638A>C | XP_011507979.1:p.Asp213Ala | |
| XM_011509678.1:c.638A>C | XP_011507980.1:p.Asp213Ala | |
| XM_011509679.1:c.638A>C | XP_011507981.1:p.Asp213Ala | |
| XM_011509680.1:c.602A>C | XP_011507982.1:p.Asp201Ala | |
| XM_011509681.1:c.560A>C | XP_011507983.1:p.Asp187Ala | |
| XM_011509682.1:c.344A>C | XP_011507984.1:p.Asp115Ala | |
| XR_921850.1:n.1065A>C | ||
| NM_000309.4:c.1046A>C | NP_000300.1:p.Asp349Ala | |
| NM_001122764.3:c.1046A>C MANE Select | NP_001116236.1:p.Asp349Ala | |
| NM_001350128.1:c.947A>C | NP_001337057.1:p.Asp316Ala | |
| NM_001350129.1:c.638A>C | NP_001337058.1:p.Asp213Ala | |
| NM_001350130.1:c.560A>C | NP_001337059.1:p.Asp187Ala | |
| NM_001350131.1:c.560A>C | NP_001337060.1:p.Asp187Ala | |
| XM_005245291.4:c.1046A>C | XP_005245348.2:p.Asp349Ala | |
| XM_006711404.4:c.1175A>C | XP_006711467.2:p.Asp392Ala | |
| XM_011509663.2:c.1175A>C | XP_011507965.1:p.Asp392Ala | |
| XM_011509665.2:c.1175A>C | XP_011507967.1:p.Asp392Ala | |
| XM_011509666.2:c.1117-153A>C | XP_011507968.1:n.1117-153A>C | |
| XM_011509667.2:c.1061A>C | XP_011507969.1:p.Asp354Ala | |
| XM_011509668.2:c.1061A>C | XP_011507970.1:p.Asp354Ala | |
| XM_011509670.2:c.1061A>C | XP_011507972.1:p.Asp354Ala | |
| XM_011509672.3:c.1061A>C | XP_011507974.1:p.Asp354Ala | |
| XM_011509673.2:c.911A>C | XP_011507975.1:p.Asp304Ala | |
| XM_011509674.2:c.937-153A>C | XP_011507976.1:n.937-153A>C | |
| XM_017001559.1:c.1117-153A>C | XP_016857048.1:n.1117-153A>C | |
| XM_017001560.2:c.988-153A>C | XP_016857049.1:n.988-153A>C | |
| XM_017001562.1:c.638A>C | XP_016857051.1:p.Asp213Ala | |
| XM_017001563.2:c.560A>C | XP_016857052.1:p.Asp187Ala | |
| XM_017001564.1:c.560A>C | XP_016857053.1:p.Asp187Ala | |
| XM_017001566.2:c.638A>C | XP_016857055.1:p.Asp213Ala | |
| XM_017001567.1:c.638A>C | XP_016857056.1:p.Asp213Ala | |
| XM_017001570.1:c.344A>C | XP_016857059.1:p.Asp115Ala | |
| XM_017001571.1:c.337-153A>C | XP_016857060.1:n.337-153A>C | |
| XM_024447863.1:c.1046A>C | XP_024303631.1:p.Asp349Ala | |
| XM_024447864.1:c.911A>C | XP_024303632.1:p.Asp304Ala | |
| XM_024447865.1:c.638A>C | XP_024303633.1:p.Asp213Ala | |
| XM_024447866.1:c.638A>C | XP_024303634.1:p.Asp213Ala | |
| XM_024447867.1:c.638A>C | XP_024303635.1:p.Asp213Ala | |
| XM_024447874.1:c.638A>C | XP_024303642.1:p.Asp213Ala | |
| XM_024447877.1:c.560A>C | XP_024303645.1:p.Asp187Ala | |
| XR_921850.2:n.1279A>C | ||
| NM_000309.5:c.1046A>C | NP_000300.1:p.Asp349Ala | |
| NM_001350128.2:c.947A>C | NP_001337057.1:p.Asp316Ala | |
| NM_001350129.2:c.638A>C | NP_001337058.1:p.Asp213Ala | |
| NM_001350130.2:c.560A>C | NP_001337059.1:p.Asp187Ala | |
| NM_001350131.2:c.560A>C | NP_001337060.1:p.Asp187Ala | |
| NM_001365398.1:c.1046A>C | NP_001352327.1:p.Asp349Ala | |
| NM_001365399.1:c.988-153A>C | NP_001352328.1:n.988-153A>C | |
| NM_001365400.1:c.638A>C | NP_001352329.1:p.Asp213Ala | |
| NM_001365401.1:c.560A>C | NP_001352330.1:p.Asp187Ala |