MyVariant.info:
GRCh37
chr5:g.156898710G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157471702G>T , CM000667.2:g.157471702G>T | GRCh38 |
| NC_000005.9:g.156898710G>T , CM000667.1:g.156898710G>T | GRCh37 |
| NC_000005.8:g.156831288G>T | NCBI36 |
| NG_016626.1:g.16684G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311946.8:c.471G>T (NIPAL4) MANE Select | ENSP00000311687.8:p.Leu157= | |
| ENST00000435489.7:c.414G>T (NIPAL4) | ENSP00000406456.3:p.Leu138= | |
| ENST00000311946.7:c.657G>T (NIPAL4) | ENSP00000311687.7:p.Leu219= | |
| ENST00000435489.6:c.600G>T (NIPAL4) | ENSP00000406456.2:p.Leu200= | |
| ENST00000517951.5:c.*1741+16563C>A (ADAM19) | ENSP00000428376.1:n.*1741+16563C>A | |
| ENST00000519150.1:c.569G>T (NIPAL4) | ENSP00000430810.1:n.569G>T | |
| NM_001099287.1:c.657G>T (NIPAL4) | NP_001092757.1:p.Leu219= | |
| NM_001172292.1:c.600G>T (NIPAL4) | NP_001165763.1:p.Leu200= | |
| XM_011534552.1:c.162G>T (NIPAL4) | XP_011532854.1:p.Leu54= | |
| XM_024446043.1:c.-43G>T (NIPAL4) | XP_024301811.1:n.-43G>T | |
| NM_001099287.2:c.471G>T (NIPAL4) MANE Select | NP_001092757.2:p.Leu157= |