COSMIC:
COSM6351653 (not active)
Revel Score:
ENST00000534313 (MANE Select)
0.163
ENST00000527525
0.163
ENST00000394224
0.163
ENST00000394227
0.163
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.0446012 (EAS)
Genomes Max Group AF
0.02338266 (EAS)
Exomes Max Group AF
0.04695915 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65641237G>T , CM000673.2:g.65641237G>T | GRCh38 |
| NC_000011.9:g.65408708G>T , CM000673.1:g.65408708G>T | GRCh37 |
| NC_000011.8:g.65165284G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000534313.6:c.316G>T MANE Select | ENSP00000436269.1:p.Ala106Ser | |
| ENST00000394224.3:c.316G>T | ENSP00000377771.3:p.Ala106Ser | |
| ENST00000394227.7:c.316G>T | ENSP00000377774.4:p.Ala106Ser | |
| ENST00000527525.5:c.316G>T | ENSP00000433686.1:p.Ala106Ser | |
| ENST00000534313.5:c.316G>T | ENSP00000436269.1:p.Ala106Ser | |
| ENST00000628801.2:c.316G>T | ENSP00000485899.1:p.Ala106Ser | |
| NM_006747.3:c.316G>T | NP_006738.3:p.Ala106Ser | |
| NM_153253.29:c.316G>T | NP_694985.29:p.Ala106Ser | |
| XM_005274189.2:c.316G>T | XP_005274246.1:p.Ala106Ser | |
| XM_011545214.1:c.316G>T | XP_011543516.1:p.Ala106Ser | |
| XR_247210.2:n.425G>T | ||
| XR_950017.1:n.425G>T | ||
| NM_006747.4:c.316G>T MANE Select | NP_006738.3:p.Ala106Ser | |
| NM_153253.30:c.316G>T | NP_694985.29:p.Ala106Ser |