MutSpliceDB:
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30888857C>G , CM000678.2:g.30888857C>G | GRCh38 |
| NC_000016.9:g.30900178C>G , CM000678.1:g.30900178C>G | GRCh37 |
| NC_000016.8:g.30807679C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215115.5:c.528+3G>C (BCL7C) MANE Select | ENSP00000215115.4:n.528+3G>C | |
| ENST00000215115.4:c.528+3G>C (BCL7C) | ENSP00000215115.4:n.528+3G>C | |
| ENST00000380317.8:c.528+3G>C (BCL7C) | ENSP00000369674.4:n.528+3G>C | |
| ENST00000572628.5:c.526+3G>C (BCL7C) | ||
| ENST00000574418.5:c.*71+3G>C (BCL7C) | ENSP00000461177.1:n.*71+3G>C | |
| NM_001286526.1:c.528+3G>C (BCL7C) | NP_001273455.1:n.528+3G>C | |
| NM_004765.3:c.528+3G>C (BCL7C) | NP_004756.2:n.528+3G>C | |
| NR_110940.1:n.803C>G (MIR762HG) | ||
| NR_110941.1:n.660-5691C>G (MIR762HG) | ||
| NR_110942.1:n.117-5691C>G (MIR762HG) | ||
| XM_011545980.1:c.528+3G>C (BCL7C) | XP_011544282.1:n.528+3G>C | |
| XM_011545980.3:c.528+3G>C (BCL7C) | XP_011544282.1:n.528+3G>C | |
| XM_017023885.2:c.*1+3G>C (BCL7C) | XP_016879374.1:n.*1+3G>C | |
| XM_017023886.2:c.*1+3G>C (BCL7C) | XP_016879375.1:n.*1+3G>C | |
| XM_017023887.2:c.*1+3G>C (BCL7C) | XP_016879376.1:n.*1+3G>C | |
| XM_017023888.2:c.*1+3G>C (BCL7C) | XP_016879377.1:n.*1+3G>C | |
| NM_001286526.2:c.528+3G>C (BCL7C) | NP_001273455.1:n.528+3G>C | |
| NM_004765.4:c.528+3G>C (BCL7C) MANE Select | NP_004756.2:n.528+3G>C |