Linked Data
ClinVar Variation Id:
1734018
ClinVar RCV Id:
RCV002348865
dbSNP Id:
rs1376620210
gnomAD v2:
7-44185199-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44145600C>T , CM000669.2:g.44145600C>T | GRCh38 |
| NC_000007.13:g.44185199C>T , CM000669.1:g.44185199C>T | GRCh37 |
| NC_000007.12:g.44151724C>T | NCBI36 |
| NG_008847.1:g.48824G>A | |
| NG_008847.2:g.57571G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*1148G>A | ENSP00000379142.4:n.*1148G>A | |
| ENST00000616242.5:c.*270G>A | ENSP00000482149.2:n.*270G>A | |
| ENST00000683378.1:n.376G>A | ||
| ENST00000336642.9:c.184G>A | ENSP00000338009.5:p.Ala62Thr | |
| ENST00000345378.7:c.1153G>A | ENSP00000223366.2:p.Ala385Thr | |
| ENST00000403799.8:c.1150G>A MANE Select | ENSP00000384247.3:p.Ala384Thr | |
| ENST00000671824.1:c.1213G>A | ENSP00000500264.1:p.Ala405Thr | |
| ENST00000672743.1:n.162G>A | ||
| ENST00000673284.1:c.1150G>A | ENSP00000499852.1:p.Ala384Thr | |
| ENST00000336642.8:c.202G>A | ENSP00000338009.4:p.Ala68Thr | |
| ENST00000345378.6:c.1153G>A | ENSP00000223366.2:p.Ala385Thr | |
| ENST00000395796.7:c.1147G>A | ENSP00000379142.3:p.Ala383Thr | |
| ENST00000403799.7:c.1150G>A | ENSP00000384247.3:p.Ala384Thr | |
| ENST00000437084.1:c.1099G>A | ENSP00000402840.1:p.Ala367Thr | |
| ENST00000459642.1:n.530G>A | ||
| ENST00000616242.4:c.1147G>A | ENSP00000482149.1:p.Ala383Thr | |
| NM_000162.3:c.1150G>A | NP_000153.1:p.Ala384Thr | |
| NM_033507.1:c.1153G>A | NP_277042.1:p.Ala385Thr | |
| NM_033508.1:c.1147G>A | NP_277043.1:p.Ala383Thr | |
| NM_000162.4:c.1150G>A | NP_000153.1:p.Ala384Thr | |
| NM_001354800.1:c.1150G>A | NP_001341729.1:p.Ala384Thr | |
| NM_001354801.1:c.139G>A | NP_001341730.1:p.Ala47Thr | |
| NM_001354802.1:c.10G>A | NP_001341731.1:p.Ala4Thr | |
| NM_001354803.1:c.184G>A | NP_001341732.1:p.Ala62Thr | |
| NM_033507.2:c.1153G>A | NP_277042.1:p.Ala385Thr | |
| NM_033508.2:c.1147G>A | NP_277043.1:p.Ala383Thr | |
| XM_024446707.1:c.10G>A | XP_024302475.1:p.Ala4Thr | |
| NM_000162.5:c.1150G>A MANE Select | NP_000153.1:p.Ala384Thr | |
| NM_033507.3:c.1153G>A | NP_277042.1:p.Ala385Thr | |
| NM_033508.3:c.1147G>A | NP_277043.1:p.Ala383Thr | |
| NM_001354803.2:c.184G>A | NP_001341732.1:p.Ala62Thr |