Linked Data
ClinVar Variation Id:
225121
dbSNP Id:
rs879255593
gnomAD v4:
3-193662936-C-T
PubMed:
PMID:25012220
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.193662936C>T , CM000665.2:g.193662936C>T | GRCh38 |
| NC_000003.11:g.193380725C>T , CM000665.1:g.193380725C>T | GRCh37 |
| NC_000003.10:g.194863419C>T | NCBI36 |
| NG_011605.1:g.74793C>T , LRG_337:g.74793C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361510.8:c.2635C>T MANE Select | ENSP00000355324.2:p.Arg879Ter | |
| ENST00000361828.7:c.2470C>T | ENSP00000354429.3:p.Arg824Ter | |
| ENST00000361908.8:c.2581C>T | ENSP00000354681.3:p.Arg861Ter | |
| ENST00000392436.7:c.2470C>T | ENSP00000376231.3:p.Arg824Ter | |
| ENST00000392437.6:c.2524C>T | ENSP00000376232.2:p.Arg842Ter | |
| ENST00000642289.1:c.2409C>T | ||
| ENST00000642445.1:c.2470C>T | ENSP00000495535.1:p.Arg824Ter | |
| ENST00000642593.1:c.*695C>T | ENSP00000494273.1:n.*695C>T | |
| ENST00000643329.1:c.2152C>T | ENSP00000493673.1:p.Arg718Ter | |
| ENST00000643737.1:c.*2551C>T | ENSP00000494210.1:n.*2551C>T | |
| ENST00000644595.1:c.2470C>T | ENSP00000494121.1:p.Arg824Ter | |
| ENST00000644629.1:c.2057C>T | ||
| ENST00000644841.1:c.*954C>T | ENSP00000493988.1:n.*954C>T | |
| ENST00000644959.1:c.2464C>T | ||
| ENST00000645553.1:c.2485C>T | ENSP00000494725.1:p.Arg829Ter | |
| ENST00000646085.1:c.*1948C>T | ENSP00000494509.1:n.*1948C>T | |
| ENST00000646277.1:c.*1071C>T | ENSP00000495289.1:n.*1071C>T | |
| ENST00000646544.1:c.1458C>T | ||
| ENST00000646699.1:c.2409C>T | ||
| ENST00000646793.1:c.2362C>T | ENSP00000494512.1:p.Arg788Ter | |
| ENST00000361150.6:c.2473C>T | ENSP00000354781.2:p.Arg825Ter | |
| ENST00000361510.6:c.2635C>T | ENSP00000355324.2:p.Arg879Ter | |
| ENST00000361715.6:c.2527C>T | ENSP00000355311.2:p.Arg843Ter | |
| ENST00000361828.6:c.2524C>T | ENSP00000354429.2:p.Arg842Ter | |
| ENST00000361908.7:c.2581C>T | ENSP00000354681.3:p.Arg861Ter | |
| ENST00000392438.7:c.2470C>T | ENSP00000376233.3:p.Arg824Ter | |
| ENST00000445863.1:c.46C>T | ENSP00000398358.1:p.Arg16Ter | |
| NM_015560.2:c.2470C>T , LRG_337t1:c.2470C>T | NP_056375.2:p.Arg824Ter | |
| NM_130831.2:c.2362C>T | NP_570844.1:p.Arg788Ter | |
| NM_130832.2:c.2416C>T | NP_570845.1:p.Arg806Ter | |
| NM_130833.2:c.2473C>T | NP_570846.1:p.Arg825Ter | |
| NM_130834.2:c.2524C>T | NP_570847.2:p.Arg842Ter | |
| NM_130835.2:c.2527C>T | NP_570848.1:p.Arg843Ter | |
| NM_130836.2:c.2581C>T | NP_570849.2:p.Arg861Ter | |
| NM_130837.2:c.2635C>T , LRG_337t2:c.2635C>T | NP_570850.2:p.Arg879Ter | |
| XM_011512863.1:c.2635C>T | XP_011511165.1:p.Arg879Ter | |
| XM_011512864.1:c.2581C>T | XP_011511166.1:p.Arg861Ter | |
| XM_011512865.1:c.2524C>T | XP_011511167.1:p.Arg842Ter | |
| XM_011512866.1:c.2473C>T | XP_011511168.1:p.Arg825Ter | |
| XM_011512867.1:c.2470C>T | XP_011511169.1:p.Arg824Ter | |
| XM_011512868.1:c.2362C>T | XP_011511170.1:p.Arg788Ter | |
| XR_924835.1:n.582+5984G>A | ||
| NM_001354663.1:c.2101C>T | NP_001341592.1:p.Arg701Ter | |
| NM_001354664.1:c.2098C>T | NP_001341593.1:p.Arg700Ter | |
| XR_001740158.2:n.2889C>T | ||
| XR_001740159.2:n.2724C>T | ||
| XR_001741072.1:n.601-2851G>A | ||
| XR_001741074.1:n.475+7872G>A | ||
| XR_924835.2:n.600+5984G>A | ||
| NM_001354663.2:c.2101C>T | NP_001341592.1:p.Arg701Ter | |
| NM_001354664.2:c.2098C>T | NP_001341593.1:p.Arg700Ter | |
| NM_130831.3:c.2362C>T | NP_570844.1:p.Arg788Ter | |
| NM_130832.3:c.2416C>T | NP_570845.1:p.Arg806Ter | |
| NM_130834.3:c.2524C>T | NP_570847.2:p.Arg842Ter | |
| NM_130836.3:c.2581C>T | NP_570849.2:p.Arg861Ter | |
| NM_015560.3:c.2470C>T | NP_056375.2:p.Arg824Ter | |
| NM_130833.3:c.2473C>T | NP_570846.1:p.Arg825Ter | |
| NM_130835.3:c.2527C>T | NP_570848.1:p.Arg843Ter | |
| NM_130837.3:c.2635C>T MANE Select | NP_570850.2:p.Arg879Ter |