ClinVar Variation:
COSMIC:
dbSNP:
Revel Score:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21971025G>C , CM000671.2:g.21971025G>C | GRCh38 |
| NC_000009.11:g.21971024G>C , CM000671.1:g.21971024G>C | GRCh37 |
| NC_000009.10:g.21961024G>C | NCBI36 |
| NG_007485.1:g.28467C>G , LRG_11:g.28467C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304494.10:c.334C>G MANE Select | ENSP00000307101.5:p.Arg112Gly | |
| ENST00000404796.3:c.348-58408G>C | ENSP00000385916.2:n.348-58408G>C | |
| ENST00000579755.2:c.377C>G MANE Plus Clinical | ENSP00000462950.1:p.Pro126Arg | |
| ENST00000304494.9:c.334C>G | ENSP00000307101.5:p.Arg112Gly | |
| ENST00000361570.4:c.376C>G | ENSP00000355153.4:p.Arg126Gly | |
| ENST00000380150.2:n.308C>G | ||
| ENST00000380151.3:c.608C>G | ENSP00000369496.3:n.608C>G | |
| ENST00000404796.2:c.348-58408G>C | ENSP00000385916.2:n.348-58408G>C | |
| ENST00000479692.2:c.181C>G | ENSP00000466887.1:p.Arg61Gly | |
| ENST00000494262.5:c.181C>G | ENSP00000464952.1:p.Arg61Gly | |
| ENST00000497750.1:c.181C>G | ENSP00000468510.1:p.Arg61Gly | |
| ENST00000498124.1:c.334C>G | ENSP00000418915.1:p.Arg112Gly | |
| ENST00000498628.6:c.181C>G | ENSP00000467857.1:p.Arg61Gly | |
| ENST00000530628.2:c.377C>G | ENSP00000432664.2:p.Pro126Arg | |
| ENST00000578845.2:c.181C>G | ENSP00000467390.1:p.Arg61Gly | |
| ENST00000579122.1:c.334C>G | ENSP00000464202.1:p.Arg112Gly | |
| ENST00000579755.1:c.377C>G | ENSP00000462950.1:p.Pro126Arg | |
| NM_000077.4:c.334C>G , LRG_11t1:c.334C>G | NP_000068.1:p.Arg112Gly | |
| NM_001195132.1:c.334C>G | NP_001182061.1:p.Arg112Gly | |
| NM_058195.3:c.377C>G , LRG_11t2:c.377C>G | NP_478102.2:p.Pro126Arg | |
| NM_058197.4:c.608C>G | NP_478104.2:n.608C>G | |
| XM_005251343.1:c.181C>G | XP_005251400.1:p.Arg61Gly | |
| XM_011517675.1:c.334C>G | XP_011515977.1:p.Arg112Gly | |
| XM_011517676.1:c.334C>G | XP_011515978.1:p.Arg112Gly | |
| XM_011517679.1:c.181C>G | XP_011515981.1:p.Arg61Gly | |
| XR_929159.1:n.735C>G | ||
| XR_929161.1:n.524C>G | ||
| XR_929162.1:n.524C>G | ||
| XR_929163.1:n.473C>G | ||
| XR_929164.1:n.256C>G | ||
| NM_001363763.1:c.181C>G | NP_001350692.1:p.Arg61Gly | |
| XM_011517675.2:c.334C>G | XP_011515977.1:p.Arg112Gly | |
| XM_011517676.2:c.334C>G | XP_011515978.1:p.Arg112Gly | |
| XR_929159.2:n.664C>G | ||
| NM_001363763.2:c.181C>G | NP_001350692.1:p.Arg61Gly | |
| NM_000077.5:c.334C>G MANE Select | NP_000068.1:p.Arg112Gly | |
| NM_001195132.2:c.334C>G | NP_001182061.1:p.Arg112Gly | |
| NM_058195.4:c.377C>G MANE Plus Clinical | NP_478102.2:p.Pro126Arg | |
| NM_058197.5:c.*257C>G | NP_478104.2:n.*257C>G |