MyVariant.info:
GRCh37
chr5:g.156898806T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471798T>C , CM000667.2:g.157471798T>C | GRCh38 |
| NC_000005.9:g.156898806T>C , CM000667.1:g.156898806T>C | GRCh37 |
| NC_000005.8:g.156831384T>C | NCBI36 |
| NG_016626.1:g.16780T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.567T>C (NIPAL4) MANE Select | ENSP00000311687.8:p.Ala189= | |
| ENST00000435489.7:c.510T>C (NIPAL4) | ENSP00000406456.3:p.Ala170= | |
| ENST00000311946.7:c.753T>C (NIPAL4) | ENSP00000311687.7:p.Ala251= | |
| ENST00000435489.6:c.696T>C (NIPAL4) | ENSP00000406456.2:p.Ala232= | |
| ENST00000517951.5:c.*1741+16467A>G (ADAM19) | ENSP00000428376.1:n.*1741+16467A>G | |
| ENST00000519150.1:c.665T>C (NIPAL4) | ENSP00000430810.1:n.665T>C | |
| NM_001099287.1:c.753T>C (NIPAL4) | NP_001092757.1:p.Ala251= | |
| NM_001172292.1:c.696T>C (NIPAL4) | NP_001165763.1:p.Ala232= | |
| XM_011534552.1:c.258T>C (NIPAL4) | XP_011532854.1:p.Ala86= | |
| XM_024446043.1:c.54T>C (NIPAL4) | XP_024301811.1:p.Ala18= | |
| NM_001099287.2:c.567T>C (NIPAL4) MANE Select | NP_001092757.2:p.Ala189= |