Linked Data
ClinVar Variation Id:
533700
dbSNP Id:
rs1557045250
gnomAD v2:
X-152959363-C-T
gnomAD v4:
X-153693908-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153693908C>T , CM000685.2:g.153693908C>T | GRCh38 |
| NC_000023.10:g.152959363C>T , CM000685.1:g.152959363C>T | GRCh37 |
| NC_000023.9:g.152612557C>T | NCBI36 |
| NG_012016.1:g.10612C>T | |
| NG_012016.2:g.10612C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.1145C>T MANE Select | ENSP00000253122.5:p.Pro382Leu | |
| ENST00000253122.9:c.1145C>T | ENSP00000253122.5:p.Pro382Leu | |
| ENST00000413787.1:c.258-296C>T | ENSP00000400463.1:n.258-296C>T | |
| ENST00000430077.6:c.800C>T | ENSP00000403041.2:p.Pro267Leu | |
| ENST00000442457.1:c.199C>T | ||
| ENST00000457723.1:c.129C>T | ENSP00000394742.1:p.Ala43= | |
| ENST00000467402.1:n.244C>T | ||
| ENST00000485324.1:n.1178C>T | ||
| NM_001142805.1:c.1115C>T | NP_001136277.1:p.Pro372Leu | |
| NM_001142806.1:c.800C>T | NP_001136278.1:p.Pro267Leu | |
| NM_005629.3:c.1145C>T | NP_005620.1:p.Pro382Leu | |
| NM_005629.4:c.1145C>T MANE Select | NP_005620.1:p.Pro382Leu | |
| NM_001142805.2:c.1115C>T | NP_001136277.1:p.Pro372Leu |