Linked Data
dbSNP Id:
rs1047993053
gnomAD v2:
19-18980111-G-T
gnomAD v3:
19-18869302-G-T
gnomAD v4:
19-18869302-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18869302G>T , CM000681.2:g.18869302G>T | GRCh38 |
| NC_000019.9:g.18980111G>T , CM000681.1:g.18980111G>T | GRCh37 |
| NC_000019.8:g.18841111G>T | NCBI36 |
| NG_012070.1:g.31843C>A | |
| NG_033056.1:g.31843C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623882.4:c.*683C>A (CERS1) MANE Select | ENSP00000485308.1:n.*683C>A | |
| ENST00000247005.8:c.414C>A (GDF1) MANE Select | ENSP00000247005.5:p.Pro138= | |
| ENST00000247005.7:c.414C>A (GDF1) | ENSP00000247005.5:p.Pro138= | |
| ENST00000623882.3:c.*683C>A (CERS1) | ENSP00000485308.1:n.*683C>A | |
| ENST00000623927.1:c.414C>A (CERS1) | ENSP00000485582.1:p.Pro138= | |
| NM_001492.5:c.414C>A (GDF1) | NP_001483.3:p.Pro138= | |
| NM_021267.4:c.*683C>A (CERS1) | NP_067090.1:n.*683C>A | |
| NM_001492.6:c.414C>A (GDF1) MANE Select | NP_001483.3:p.Pro138= | |
| NM_021267.5:c.*683C>A (CERS1) MANE Select | NP_067090.1:n.*683C>A | |
| NM_001387438.1:c.414C>A (GDF1) | NP_001374367.1:p.Pro138= | |
| NM_001387440.1:c.*1275C>A (CERS1) | NP_001374369.1:n.*1275C>A |