Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100119693A>G , CM000669.2:g.100119693A>G | GRCh38 |
| NC_000007.13:g.99717316A>G , CM000669.1:g.99717316A>G | GRCh37 |
| NC_000007.12:g.99555252A>G | NCBI36 |
| NG_029454.1:g.5166T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262932.5:c.-52A>G (CNPY4) MANE Select | ENSP00000262932.3:n.-52A>G | |
| ENST00000262932.4:c.-52A>G (CNPY4) | ENSP00000262932.3:n.-52A>G | |
| ENST00000437822.6:c.52+2T>C (TAF6) | ENSP00000399982.2:n.52+2T>C | |
| NM_001190415.1:c.52+2T>C (TAF6) | NP_001177344.1:n.52+2T>C | |
| NM_152755.1:c.-52A>G (CNPY4) | NP_689968.1:n.-52A>G | |
| XM_024446896.1:c.-59-5425T>C (TAF6) | XP_024302664.1:n.-59-5425T>C | |
| NM_152755.2:c.-52A>G (CNPY4) MANE Select | NP_689968.1:n.-52A>G | |
| NM_001190415.2:c.52+2T>C (TAF6) | NP_001177344.1:n.52+2T>C |