Linked Data
ClinVar Variation Id:
1528611
ClinVar RCV Id:
RCV002077565
dbSNP Id:
rs771594642
ExAC:
X:43817850 G / A
gnomAD v2:
X-43817850-G-A
gnomAD v4:
X-43958604-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43958604G>A , CM000685.2:g.43958604G>A | GRCh38 |
| NC_000023.10:g.43817850G>A , CM000685.1:g.43817850G>A | GRCh37 |
| NC_000023.9:g.43702794G>A | NCBI36 |
| NG_009832.1:g.20072C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642620.1:c.42C>T (NDP) MANE Select | ENSP00000495972.1:p.Ser14= | |
| ENST00000647044.1:c.42C>T (NDP) | ENSP00000495811.1:p.Ser14= | |
| ENST00000378062.5:c.42C>T (NDP) | ENSP00000367301.5:p.Ser14= | |
| ENST00000470584.1:n.218+114C>T (NDP) | ||
| NM_000266.3:c.42C>T (NDP) | NP_000257.1:p.Ser14= | |
| NR_046631.1:n.467-2181G>A (NDP-AS1) | ||
| NM_000266.4:c.42C>T (NDP) MANE Select | NP_000257.1:p.Ser14= |