Linked Data
ClinVar Variation Id:
376526
dbSNP Id:
rs1057519956
COSMIC:
COSM3577726
PubMed:
PMID:26619011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218583025T>C , CM000664.2:g.218583025T>C | GRCh38 |
| NC_000002.11:g.219447748T>C , CM000664.1:g.219447748T>C | GRCh37 |
| NC_000002.10:g.219155992T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000273064.11:c.259T>C MANE Select | ENSP00000273064.6:p.Ser87Pro | |
| ENST00000273064.10:c.259T>C | ENSP00000273064.6:p.Ser87Pro | |
| ENST00000295701.9:c.259T>C | ENSP00000295701.5:p.Ser87Pro | |
| ENST00000432877.5:c.*151T>C | ENSP00000392394.1:n.*151T>C | |
| ENST00000542068.5:c.259T>C | ENSP00000443687.1:p.Ser87Pro | |
| ENST00000627282.2:c.259T>C | ENSP00000486540.1:p.Ser87Pro | |
| NM_001271634.1:c.259T>C | NP_001258563.1:p.Ser87Pro | |
| NM_001271635.1:c.259T>C | NP_001258564.1:p.Ser87Pro | |
| NM_005444.2:c.259T>C | NP_005435.1:p.Ser87Pro | |
| NR_073390.1:n.634T>C | ||
| XM_011512138.1:c.100T>C | XP_011510440.1:p.Ser34Pro | |
| XM_011512138.3:c.100T>C | XP_011510440.1:p.Ser34Pro | |
| XM_017005248.1:c.97T>C | XP_016860737.1:p.Ser33Pro | |
| XM_017005249.2:c.100T>C | XP_016860738.1:p.Ser34Pro | |
| NM_001271634.2:c.259T>C | NP_001258563.1:p.Ser87Pro | |
| NM_005444.3:c.259T>C MANE Select | NP_005435.1:p.Ser87Pro | |
| NR_073390.2:n.375T>C | ||
| NM_001271635.2:c.259T>C | NP_001258564.1:p.Ser87Pro |