Linked Data
ClinVar Variation Id:
1256784
ClinVar RCV Id:
RCV001673393
dbSNP Id:
rs3735273
ExAC:
7:50596864 C / T
gnomAD v2:
7-50596864-C-T
gnomAD v3:
7-50529166-C-T
gnomAD v4:
7-50529166-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.50529166C>T , CM000669.2:g.50529166C>T | GRCh38 |
| NC_000007.13:g.50596864C>T , CM000669.1:g.50596864C>T | GRCh37 |
| NC_000007.12:g.50564358C>T | NCBI36 |
| NG_008742.1:g.41291G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000444124.7:c.570+42G>A (DDC) MANE Select | ENSP00000403644.2:n.570+42G>A | |
| ENST00000357936.9:c.570+42G>A (DDC) | ENSP00000350616.5:n.570+42G>A | |
| ENST00000380984.4:c.570+42G>A (DDC) | ENSP00000370371.4:n.570+42G>A | |
| ENST00000426377.5:c.336+42G>A (DDC) | ENSP00000395069.1:n.336+42G>A | |
| ENST00000430300.5:c.213-886G>A (DDC) | ||
| ENST00000431062.5:c.435+8694G>A (DDC) | ENSP00000399184.1:n.435+8694G>A | |
| ENST00000444124.6:c.570+42G>A (DDC) | ENSP00000403644.2:n.570+42G>A | |
| ENST00000444733.5:c.456+42G>A (DDC) | ENSP00000393724.1:n.456+42G>A | |
| ENST00000489162.1:n.369+42G>A (DDC) | ||
| ENST00000613602.3:c.-11+13352G>A (FIGNL1) | ENSP00000481751.1:n.-11+13352G>A | |
| ENST00000615193.4:c.435+8694G>A (DDC) | ENSP00000484104.1:n.435+8694G>A | |
| ENST00000617822.4:c.570+42G>A (DDC) | ENSP00000478385.1:n.570+42G>A | |
| ENST00000622873.4:c.456+42G>A (DDC) | ENSP00000479110.1:n.456+42G>A | |
| NM_000790.3:c.570+42G>A (DDC) | NP_000781.1:n.570+42G>A | |
| NM_001082971.1:c.570+42G>A (DDC) | NP_001076440.1:n.570+42G>A | |
| NM_001242886.1:c.456+42G>A (DDC) | NP_001229815.1:n.456+42G>A | |
| NM_001242887.1:c.570+42G>A (DDC) | NP_001229816.1:n.570+42G>A | |
| NM_001242888.1:c.336+42G>A (DDC) | NP_001229817.1:n.336+42G>A | |
| NM_001242889.1:c.435+8694G>A (DDC) | NP_001229818.1:n.435+8694G>A | |
| NM_001242890.1:c.570+42G>A (DDC) | NP_001229819.1:n.570+42G>A | |
| XM_005271745.3:c.456+42G>A (DDC) | XP_005271802.1:n.456+42G>A | |
| XM_011515161.1:c.219+42G>A (DDC) | XP_011513463.1:n.219+42G>A | |
| XM_005271745.4:c.456+42G>A (DDC) | XP_005271802.1:n.456+42G>A | |
| XM_011515161.2:c.513+42G>A (DDC) | XP_011513463.2:n.513+42G>A | |
| NM_001082971.2:c.570+42G>A (DDC) MANE Select | NP_001076440.2:n.570+42G>A | |
| NM_000790.4:c.570+42G>A (DDC) | NP_000781.2:n.570+42G>A | |
| NM_001242888.2:c.336+42G>A (DDC) | NP_001229817.2:n.336+42G>A | |
| NM_001242890.2:c.570+42G>A (DDC) | NP_001229819.2:n.570+42G>A | |
| NM_001242886.2:c.456+42G>A (DDC) | NP_001229815.2:n.456+42G>A | |
| NM_001242887.2:c.570+42G>A (DDC) | NP_001229816.2:n.570+42G>A | |
| NM_001242889.2:c.435+8694G>A (DDC) | NP_001229818.2:n.435+8694G>A |