MyVariant.info:
GRCh37
chr5:g.156898809C>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471801C>G , CM000667.2:g.157471801C>G | GRCh38 |
| NC_000005.9:g.156898809C>G , CM000667.1:g.156898809C>G | GRCh37 |
| NC_000005.8:g.156831387C>G | NCBI36 |
| NG_016626.1:g.16783C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.570C>G (NIPAL4) MANE Select | ENSP00000311687.8:p.Ser190= | |
| ENST00000435489.7:c.513C>G (NIPAL4) | ENSP00000406456.3:p.Ser171= | |
| ENST00000311946.7:c.756C>G (NIPAL4) | ENSP00000311687.7:p.Ser252= | |
| ENST00000435489.6:c.699C>G (NIPAL4) | ENSP00000406456.2:p.Ser233= | |
| ENST00000517951.5:c.*1741+16464G>C (ADAM19) | ENSP00000428376.1:n.*1741+16464G>C | |
| ENST00000519150.1:c.668C>G (NIPAL4) | ENSP00000430810.1:n.668C>G | |
| NM_001099287.1:c.756C>G (NIPAL4) | NP_001092757.1:p.Ser252= | |
| NM_001172292.1:c.699C>G (NIPAL4) | NP_001165763.1:p.Ser233= | |
| XM_011534552.1:c.261C>G (NIPAL4) | XP_011532854.1:p.Ser87= | |
| XM_024446043.1:c.57C>G (NIPAL4) | XP_024301811.1:p.Ser19= | |
| NM_001099287.2:c.570C>G (NIPAL4) MANE Select | NP_001092757.2:p.Ser190= |