Linked Data
ClinVar Variation Id:
1802421
ClinVar RCV Id:
RCV003138279
gnomAD v4:
9-21971093-C-A
COSMIC:
COSM13472
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21971093C>A , CM000671.2:g.21971093C>A | GRCh38 |
| NC_000009.11:g.21971092C>A , CM000671.1:g.21971092C>A | GRCh37 |
| NC_000009.10:g.21961092C>A | NCBI36 |
| NG_007485.1:g.28399G>T , LRG_11:g.28399G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000304494.10:c.266G>T MANE Select | ENSP00000307101.5:p.Gly89Val | |
| ENST00000404796.3:c.348-58340C>A | ENSP00000385916.2:n.348-58340C>A | |
| ENST00000579755.2:c.309G>T MANE Plus Clinical | ENSP00000462950.1:p.Gly103= | |
| ENST00000304494.9:c.266G>T | ENSP00000307101.5:p.Gly89Val | |
| ENST00000361570.4:c.308G>T | ENSP00000355153.4:p.Gly103Val | |
| ENST00000380150.2:n.240G>T | ||
| ENST00000380151.3:c.540G>T | ENSP00000369496.3:n.540G>T | |
| ENST00000404796.2:c.348-58340C>A | ENSP00000385916.2:n.348-58340C>A | |
| ENST00000479692.2:c.113G>T | ENSP00000466887.1:p.Gly38Val | |
| ENST00000494262.5:c.113G>T | ENSP00000464952.1:p.Gly38Val | |
| ENST00000497750.1:c.113G>T | ENSP00000468510.1:p.Gly38Val | |
| ENST00000498124.1:c.266G>T | ENSP00000418915.1:p.Gly89Val | |
| ENST00000498628.6:c.113G>T | ENSP00000467857.1:p.Gly38Val | |
| ENST00000530628.2:c.309G>T | ENSP00000432664.2:p.Gly103= | |
| ENST00000578845.2:c.113G>T | ENSP00000467390.1:p.Gly38Val | |
| ENST00000579122.1:c.266G>T | ENSP00000464202.1:p.Gly89Val | |
| ENST00000579755.1:c.309G>T | ENSP00000462950.1:p.Gly103= | |
| NM_000077.4:c.266G>T , LRG_11t1:c.266G>T | NP_000068.1:p.Gly89Val | |
| NM_001195132.1:c.266G>T | NP_001182061.1:p.Gly89Val | |
| NM_058195.3:c.309G>T , LRG_11t2:c.309G>T | NP_478102.2:p.Gly103= | |
| NM_058197.4:c.540G>T | NP_478104.2:n.540G>T | |
| XM_005251343.1:c.113G>T | XP_005251400.1:p.Gly38Val | |
| XM_011517675.1:c.266G>T | XP_011515977.1:p.Gly89Val | |
| XM_011517676.1:c.266G>T | XP_011515978.1:p.Gly89Val | |
| XM_011517679.1:c.113G>T | XP_011515981.1:p.Gly38Val | |
| XR_929159.1:n.667G>T | ||
| XR_929161.1:n.456G>T | ||
| XR_929162.1:n.456G>T | ||
| XR_929163.1:n.405G>T | ||
| XR_929164.1:n.188G>T | ||
| NM_001363763.1:c.113G>T | NP_001350692.1:p.Gly38Val | |
| XM_011517675.2:c.266G>T | XP_011515977.1:p.Gly89Val | |
| XM_011517676.2:c.266G>T | XP_011515978.1:p.Gly89Val | |
| XR_929159.2:n.596G>T | ||
| NM_001363763.2:c.113G>T | NP_001350692.1:p.Gly38Val | |
| NM_000077.5:c.266G>T MANE Select | NP_000068.1:p.Gly89Val | |
| NM_001195132.2:c.266G>T | NP_001182061.1:p.Gly89Val | |
| NM_058195.4:c.309G>T MANE Plus Clinical | NP_478102.2:p.Gly103= | |
| NM_058197.5:c.*189G>T | NP_478104.2:n.*189G>T |