Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100124837C>G , CM000669.2:g.100124837C>G | GRCh38 |
| NC_000007.13:g.99722460C>G , CM000669.1:g.99722460C>G | GRCh37 |
| NC_000007.12:g.99560396C>G | NCBI36 |
| NG_029454.1:g.22G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262932.5:c.696C>G (CNPY4) MANE Select | ENSP00000262932.3:p.Asp232Glu | |
| ENST00000262932.4:c.696C>G (CNPY4) | ENSP00000262932.3:p.Asp232Glu | |
| ENST00000462193.2:c.660C>G (CNPY4) | ||
| ENST00000480692.4:n.785C>G (CNPY4) | ||
| NM_152755.1:c.696C>G (CNPY4) | NP_689968.1:p.Asp232Glu | |
| XM_024446896.1:c.-60+2305G>C (TAF6) | XP_024302664.1:n.-60+2305G>C | |
| NM_152755.2:c.696C>G (CNPY4) MANE Select | NP_689968.1:p.Asp232Glu |