Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100124833G>A , CM000669.2:g.100124833G>A | GRCh38 |
| NC_000007.13:g.99722456G>A , CM000669.1:g.99722456G>A | GRCh37 |
| NC_000007.12:g.99560392G>A | NCBI36 |
| NG_029454.1:g.26C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_152755.2:c.692G>A (CNPY4) MANE Select | NP_689968.1:p.Gly231Glu |
| ENST00000262932.5:c.692G>A (CNPY4) MANE Select | ENSP00000262932.3:p.Gly231Glu |
| NM_152755.1:c.692G>A (CNPY4) | NP_689968.1:p.Gly231Glu |
| ENST00000262932.4:c.692G>A (CNPY4) | ENSP00000262932.3:p.Gly231Glu |
| ENST00000462193.2:c.656G>A (CNPY4) | |
| ENST00000480692.4:n.781G>A (CNPY4) | |
| XM_024446896.1:c.-60+2309C>T (TAF6) | XP_024302664.1:n.-60+2309C>T |