Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100122552G>A , CM000669.2:g.100122552G>A | GRCh38 |
| NC_000007.13:g.99720175G>A , CM000669.1:g.99720175G>A | GRCh37 |
| NC_000007.12:g.99558111G>A | NCBI36 |
| NG_029454.1:g.2307C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262932.5:c.317G>A (CNPY4) MANE Select | ENSP00000262932.3:p.Arg106His | |
| ENST00000262932.4:c.317G>A (CNPY4) | ENSP00000262932.3:p.Arg106His | |
| ENST00000462193.2:c.199G>A (CNPY4) | ||
| ENST00000480692.4:n.406G>A (CNPY4) | ||
| ENST00000483756.5:c.-41G>A (CNPY4) | ENSP00000488362.1:n.-41G>A | |
| NM_152755.1:c.317G>A (CNPY4) | NP_689968.1:p.Arg106His | |
| XM_024446896.1:c.-60+4590C>T (TAF6) | XP_024302664.1:n.-60+4590C>T | |
| NM_152755.2:c.317G>A (CNPY4) MANE Select | NP_689968.1:p.Arg106His |