ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48130393G>C , CM000674.2:g.48130393G>C | GRCh38 |
| NC_000012.11:g.48524176G>C , CM000674.1:g.48524176G>C | GRCh37 |
| NC_000012.10:g.46810443G>C | NCBI36 |
| NG_016199.1:g.29521G>C | |
| NG_016199.2:g.30141G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000550257.7:c.338G>C | ENSP00000447997.3:p.Arg113Pro | |
| ENST00000340802.12:c.329G>C | ENSP00000345771.6:p.Arg110Pro | |
| ENST00000359794.11:c.116G>C MANE Select | ENSP00000352842.5:p.Arg39Pro | |
| ENST00000549941.7:c.116G>C | ENSP00000446829.3:p.Arg39Pro | |
| ENST00000550257.6:c.224G>C | ENSP00000447997.2:p.Arg75Pro | |
| ENST00000550345.6:c.116G>C | ENSP00000450369.2:p.Arg39Pro | |
| ENST00000550924.6:c.116G>C | ENSP00000446945.2:p.Arg39Pro | |
| ENST00000551339.6:c.116G>C | ENSP00000448253.2:p.Arg39Pro | |
| ENST00000642730.1:c.425G>C | ENSP00000496597.1:p.Arg142Pro | |
| ENST00000312352.11:c.116G>C | ENSP00000309438.7:p.Arg39Pro | |
| ENST00000340802.10:c.329G>C | ENSP00000345771.6:p.Arg110Pro | |
| ENST00000359794.9:c.116G>C | ENSP00000352842.5:p.Arg39Pro | |
| ENST00000546465.1:c.85+7534G>C | ENSP00000446519.1:n.85+7534G>C | |
| ENST00000546964.5:n.188G>C | ||
| ENST00000547066.5:c.*132G>C | ENSP00000448318.1:n.*132G>C | |
| ENST00000547581.5:c.*132G>C | ENSP00000447992.1:n.*132G>C | |
| ENST00000547587.5:c.116G>C | ENSP00000449426.1:p.Arg39Pro | |
| ENST00000548288.5:c.329G>C | ENSP00000448018.1:p.Arg110Pro | |
| ENST00000548345.5:c.116G>C | ENSP00000449269.1:p.Arg39Pro | |
| ENST00000548720.5:n.183G>C | ||
| ENST00000549003.5:c.116G>C | ENSP00000449835.1:p.Arg39Pro | |
| ENST00000549022.5:c.116G>C | ENSP00000446805.1:p.Arg39Pro | |
| ENST00000549366.5:c.425G>C | ENSP00000449622.1:p.Arg142Pro | |
| ENST00000549941.5:c.215G>C | ENSP00000446829.1:p.Arg72Pro | |
| ENST00000550257.5:c.338G>C | ENSP00000447997.1:p.Arg113Pro | |
| ENST00000550345.5:c.116G>C | ENSP00000450369.1:p.Arg39Pro | |
| ENST00000550924.5:c.116G>C | ENSP00000446945.1:p.Arg39Pro | |
| ENST00000551339.5:c.116G>C | ENSP00000448253.1:p.Arg39Pro | |
| ENST00000551485.5:c.116G>C | ENSP00000448315.1:p.Arg39Pro | |
| ENST00000551548.5:n.179G>C | ||
| ENST00000551804.5:c.116G>C | ENSP00000448177.1:p.Arg39Pro | |
| ENST00000552792.5:c.329G>C | ENSP00000448940.1:p.Arg110Pro | |
| ENST00000552989.5:c.86-3846G>C | ENSP00000447774.1:n.86-3846G>C | |
| ENST00000629846.2:c.116G>C | ENSP00000486196.1:p.Arg39Pro | |
| NM_000289.5:c.116G>C | NP_000280.1:p.Arg39Pro | |
| NM_001166686.1:c.329G>C | NP_001160158.1:p.Arg110Pro | |
| NM_001166687.1:c.116G>C | NP_001160159.1:p.Arg39Pro | |
| NM_001166688.1:c.116G>C | NP_001160160.1:p.Arg39Pro | |
| XM_005268974.1:c.425G>C | XP_005269031.1:p.Arg142Pro | |
| XM_005268975.1:c.425G>C | XP_005269032.1:p.Arg142Pro | |
| XM_005268976.2:c.425G>C | XP_005269033.1:p.Arg142Pro | |
| XM_005268977.1:c.329G>C | XP_005269034.1:p.Arg110Pro | |
| XM_005268978.2:c.329G>C | XP_005269035.1:p.Arg110Pro | |
| XM_005268979.1:c.329G>C | XP_005269036.1:p.Arg110Pro | |
| XM_011538487.1:c.425G>C | XP_011536789.1:p.Arg142Pro | |
| XM_011538488.1:c.116G>C | XP_011536790.1:p.Arg39Pro | |
| NM_000289.6:c.116G>C MANE Select | NP_000280.1:p.Arg39Pro | |
| NM_001166686.2:c.329G>C | NP_001160158.1:p.Arg110Pro | |
| NM_001354735.1:c.425G>C | NP_001341664.1:p.Arg142Pro | |
| NM_001354736.1:c.425G>C | NP_001341665.1:p.Arg142Pro | |
| NM_001354737.1:c.329G>C | NP_001341666.1:p.Arg110Pro | |
| NM_001354738.1:c.329G>C | NP_001341667.1:p.Arg110Pro | |
| NM_001354739.1:c.329G>C | NP_001341668.1:p.Arg110Pro | |
| NM_001354740.1:c.260G>C | NP_001341669.1:p.Arg87Pro | |
| NM_001354741.1:c.140G>C | NP_001341670.1:p.Arg47Pro | |
| NM_001354742.1:c.116G>C | NP_001341671.1:p.Arg39Pro | |
| NM_001354743.1:c.116G>C | NP_001341672.1:p.Arg39Pro | |
| NM_001354744.1:c.116G>C | NP_001341673.1:p.Arg39Pro | |
| NM_001354745.1:c.29G>C | NP_001341674.1:p.Arg10Pro | |
| NM_001354746.1:c.116G>C | NP_001341675.1:p.Arg39Pro | |
| NM_001354747.1:c.10-923G>C | NP_001341676.1:n.10-923G>C | |
| NM_001354748.1:c.10-923G>C | NP_001341677.1:n.10-923G>C | |
| NM_001363619.1:c.116G>C | NP_001350548.1:p.Arg39Pro | |
| NR_148954.1:n.301G>C | ||
| NR_148955.1:n.937G>C | ||
| NR_148956.1:n.271-923G>C | ||
| NR_148957.1:n.301G>C | ||
| NR_148958.1:n.301G>C | ||
| NR_148959.1:n.271-923G>C | ||
| XM_005268976.3:c.425G>C | XP_005269033.1:p.Arg142Pro | |
| XM_017019469.1:c.329G>C | XP_016874958.1:p.Arg110Pro | |
| XM_024449020.1:c.338G>C | XP_024304788.1:p.Arg113Pro | |
| XM_024449021.1:c.215G>C | XP_024304789.1:p.Arg72Pro | |
| XM_024449022.1:c.116G>C | XP_024304790.1:p.Arg39Pro | |
| NM_001166687.2:c.116G>C | NP_001160159.1:p.Arg39Pro | |
| NM_001166688.2:c.116G>C | NP_001160160.1:p.Arg39Pro | |
| NM_001354741.2:c.140G>C | NP_001341670.1:p.Arg47Pro | |
| NM_001354742.2:c.116G>C | NP_001341671.1:p.Arg39Pro | |
| NM_001354743.2:c.116G>C | NP_001341672.1:p.Arg39Pro | |
| NM_001354744.2:c.116G>C | NP_001341673.1:p.Arg39Pro | |
| NM_001354745.2:c.29G>C | NP_001341674.1:p.Arg10Pro | |
| NM_001354746.2:c.116G>C | NP_001341675.1:p.Arg39Pro | |
| NM_001354747.2:c.10-923G>C | NP_001341676.1:n.10-923G>C | |
| NM_001354748.2:c.10-923G>C | NP_001341677.1:n.10-923G>C | |
| NM_001363619.2:c.116G>C | NP_001350548.1:p.Arg39Pro | |
| NR_148954.2:n.167G>C | ||
| NR_148956.2:n.137-923G>C | ||
| NR_148957.2:n.167G>C | ||
| NR_148958.2:n.167G>C | ||
| NR_148959.2:n.137-923G>C |