Linked Data
ClinVar Variation Id:
237268
dbSNP Id:
rs745967881
ExAC:
4:55602960 C / T
gnomAD v2:
4-55602960-C-T
gnomAD v3:
4-54736794-C-T
gnomAD v4:
4-54736794-C-T
COSMIC:
COSM3301469
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54736794C>T , CM000666.2:g.54736794C>T | GRCh38 |
| NC_000004.11:g.55602960C>T , CM000666.1:g.55602960C>T | GRCh37 |
| NC_000004.10:g.55297717C>T | NCBI36 |
| NG_007456.1:g.83800C>T , LRG_307:g.83800C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.2658C>T | ENSP00000390987.3:p.Leu886= | |
| ENST00000684818.1:n.1362C>T | ||
| ENST00000685269.1:n.2748C>T | ||
| ENST00000686011.1:c.2655C>T | ENSP00000509704.1:p.Leu885= | |
| ENST00000687109.1:c.2673C>T | ENSP00000509371.1:p.Leu891= | |
| ENST00000687208.1:n.3082C>T | ||
| ENST00000687246.1:c.2535C>T | ENSP00000509114.1:p.Leu845= | |
| ENST00000687265.1:n.2828C>T | ||
| ENST00000687295.1:c.2658C>T | ENSP00000509450.1:p.Leu886= | |
| ENST00000688060.1:n.467C>T | ||
| ENST00000689832.1:c.2670C>T | ENSP00000509084.1:p.Leu890= | |
| ENST00000689994.1:c.2160C>T | ENSP00000509156.1:p.Leu720= | |
| ENST00000690543.1:c.2661C>T | ENSP00000508831.1:p.Leu887= | |
| ENST00000690917.1:n.2888C>T | ||
| ENST00000691361.1:n.1580C>T | ||
| ENST00000692301.1:n.1362C>T | ||
| ENST00000692783.1:c.2667C>T | ENSP00000508733.1:p.Leu889= | |
| ENST00000692991.1:n.2767C>T | ||
| ENST00000288135.6:c.2670C>T MANE Select | ENSP00000288135.6:p.Leu890= | |
| ENST00000288135.5:c.2670C>T | ENSP00000288135.5:p.Leu890= | |
| ENST00000412167.6:c.2658C>T | ENSP00000390987.2:p.Leu886= | |
| NM_000222.2:c.2670C>T , LRG_307t1:c.2670C>T | NP_000213.1:p.Leu890= | |
| NM_001093772.1:c.2658C>T | NP_001087241.1:p.Leu886= | |
| XM_005265740.1:c.2673C>T | XP_005265797.1:p.Leu891= | |
| XM_005265741.1:c.2670C>T | XP_005265798.1:p.Leu890= | |
| XM_005265742.1:c.2661C>T | XP_005265799.1:p.Leu887= | |
| XM_005265742.3:c.2661C>T | XP_005265799.1:p.Leu887= | |
| XM_017008178.1:c.2667C>T | XP_016863667.1:p.Leu889= | |
| XM_017008179.1:c.2658C>T | XP_016863668.1:p.Leu886= | |
| XM_017008180.1:c.2655C>T | XP_016863669.1:p.Leu885= | |
| NM_000222.3:c.2670C>T MANE Select | NP_000213.1:p.Leu890= | |
| NM_001093772.2:c.2658C>T | NP_001087241.1:p.Leu886= | |
| NM_001385284.1:c.2673C>T | NP_001372213.1:p.Leu891= | |
| NM_001385285.1:c.2667C>T | NP_001372214.1:p.Leu889= | |
| NM_001385286.1:c.2655C>T | NP_001372215.1:p.Leu885= | |
| NM_001385288.1:c.2661C>T | NP_001372217.1:p.Leu887= | |
| NM_001385290.1:c.2670C>T | NP_001372219.1:p.Leu890= | |
| NM_001385292.1:c.2658C>T | NP_001372221.1:p.Leu886= |