Linked Data
ClinVar Variation Id:
1154753
ClinVar RCV Id:
RCV001496873
dbSNP Id:
rs2146018260
gnomAD v4:
19-18880276-G-A
MyVariant Identifiers:
chr19:g.18991085G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18880276G>A , CM000681.2:g.18880276G>A | GRCh38 |
| NC_000019.9:g.18991085G>A , CM000681.1:g.18991085G>A | GRCh37 |
| NC_000019.8:g.18852085G>A | NCBI36 |
| NG_012070.1:g.20869C>T | |
| NG_033056.1:g.20869C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623882.4:c.750C>T (CERS1) MANE Select | ENSP00000485308.1:p.Ser250= | |
| ENST00000247005.8:c.-573C>T (GDF1) MANE Select | ENSP00000247005.5:n.-573C>T | |
| ENST00000247005.7:c.-573C>T (GDF1) | ENSP00000247005.5:n.-573C>T | |
| ENST00000429504.6:c.750C>T (CERS1) | ENSP00000389044.1:p.Ser250= | |
| ENST00000542296.6:c.456C>T (CERS1) | ENSP00000437648.1:p.Ser152= | |
| ENST00000596048.1:c.307C>T (CERS1) | ||
| ENST00000623882.3:c.750C>T (CERS1) | ENSP00000485308.1:p.Ser250= | |
| ENST00000623927.1:c.-573C>T (CERS1) | ENSP00000485582.1:n.-573C>T | |
| NM_001290265.1:c.456C>T (CERS1) | NP_001277194.1:p.Ser152= | |
| NM_001492.5:c.-573C>T (GDF1) | NP_001483.3:n.-573C>T | |
| NM_021267.4:c.750C>T (CERS1) | NP_067090.1:p.Ser250= | |
| NM_198207.2:c.750C>T (CERS1) | NP_937850.1:p.Ser250= | |
| NM_001492.6:c.-573C>T (GDF1) MANE Select | NP_001483.3:n.-573C>T | |
| NM_021267.5:c.750C>T (CERS1) MANE Select | NP_067090.1:p.Ser250= | |
| NM_198207.3:c.750C>T (CERS1) | NP_937850.1:p.Ser250= | |
| NM_001290265.2:c.456C>T (CERS1) | NP_001277194.1:p.Ser152= | |
| NM_001387438.1:c.-313+3811C>T (GDF1) | NP_001374367.1:n.-313+3811C>T | |
| NM_001387439.1:c.750C>T (CERS1) | NP_001374368.1:p.Ser250= | |
| NM_001387440.1:c.750C>T (CERS1) | NP_001374369.1:p.Ser250= | |
| NM_001387441.1:c.705C>T (CERS1) | NP_001374370.1:p.Ser235= | |
| NM_001387442.1:c.456C>T (CERS1) | NP_001374371.1:p.Ser152= | |
| NM_001387443.1:c.456C>T (CERS1) | NP_001374372.1:p.Ser152= | |
| NM_001387444.1:c.456C>T (CERS1) | NP_001374373.1:p.Ser152= | |
| NM_001387445.1:c.456C>T (CERS1) | NP_001374374.1:p.Ser152= |