Linked Data
ClinVar Variation Id:
141521
dbSNP Id:
rs374892194
ExAC:
5:112175769 C / T
gnomAD v2:
5-112175769-C-T
gnomAD v3:
5-112840072-C-T
gnomAD v4:
5-112840072-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840072C>T , CM000667.2:g.112840072C>T | GRCh38 |
| NC_000005.9:g.112175769C>T , CM000667.1:g.112175769C>T | GRCh37 |
| NC_000005.8:g.112203668C>T | NCBI36 |
| NG_008481.4:g.152552C>T , LRG_130:g.152552C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.4532C>T | ENSP00000473355.2:p.Thr1511Met | |
| ENST00000505350.2:c.*4484C>T | ENSP00000481752.1:n.*4484C>T | |
| ENST00000507379.6:c.4424C>T | ENSP00000423224.2:p.Thr1475Met | |
| ENST00000509732.6:c.4478C>T | ENSP00000426541.2:p.Thr1493Met | |
| ENST00000512211.7:c.4478C>T | ENSP00000423828.3:p.Thr1493Met | |
| ENST00000257430.9:c.4478C>T MANE Select | ENSP00000257430.4:p.Thr1493Met | |
| ENST00000257430.8:c.4478C>T | ENSP00000257430.4:p.Thr1493Met | |
| ENST00000508376.6:c.4478C>T | ENSP00000427089.2:p.Thr1493Met | |
| ENST00000508624.5:c.*3800C>T | ENSP00000424265.1:n.*3800C>T | |
| ENST00000520401.1:c.230+11100C>T | ||
| NM_000038.5:c.4478C>T | NP_000029.2:p.Thr1493Met | |
| NM_001127510.2:c.4478C>T | NP_001120982.1:p.Thr1493Met | |
| NM_001127511.2:c.4424C>T | NP_001120983.2:p.Thr1475Met | |
| NM_001354895.1:c.4478C>T | NP_001341824.1:p.Thr1493Met | |
| NM_001354896.1:c.4532C>T | NP_001341825.1:p.Thr1511Met | |
| NM_001354897.1:c.4508C>T | NP_001341826.1:p.Thr1503Met | |
| NM_001354898.1:c.4403C>T | NP_001341827.1:p.Thr1468Met | |
| NM_001354899.1:c.4394C>T | NP_001341828.1:p.Thr1465Met | |
| NM_001354900.1:c.4355C>T | NP_001341829.1:p.Thr1452Met | |
| NM_001354901.1:c.4301C>T | NP_001341830.1:p.Thr1434Met | |
| NM_001354902.1:c.4205C>T | NP_001341831.1:p.Thr1402Met | |
| NM_001354903.1:c.4175C>T | NP_001341832.1:p.Thr1392Met | |
| NM_001354904.1:c.4100C>T | NP_001341833.1:p.Thr1367Met | |
| NM_001354905.1:c.3998C>T | NP_001341834.1:p.Thr1333Met | |
| NM_001354906.1:c.3629C>T | NP_001341835.1:p.Thr1210Met | |
| NM_000038.6:c.4478C>T MANE Select | NP_000029.2:p.Thr1493Met | |
| NM_001127510.3:c.4478C>T | NP_001120982.1:p.Thr1493Met | |
| NM_001127511.3:c.4424C>T | NP_001120983.2:p.Thr1475Met | |
| NM_001354895.2:c.4478C>T | NP_001341824.1:p.Thr1493Met | |
| NM_001354896.2:c.4532C>T | NP_001341825.1:p.Thr1511Met | |
| NM_001354897.2:c.4508C>T | NP_001341826.1:p.Thr1503Met | |
| NM_001354898.2:c.4403C>T | NP_001341827.1:p.Thr1468Met | |
| NM_001354899.2:c.4394C>T | NP_001341828.1:p.Thr1465Met | |
| NM_001354900.2:c.4355C>T | NP_001341829.1:p.Thr1452Met | |
| NM_001354901.2:c.4301C>T | NP_001341830.1:p.Thr1434Met | |
| NM_001354902.2:c.4205C>T | NP_001341831.1:p.Thr1402Met | |
| NM_001354903.2:c.4175C>T | NP_001341832.1:p.Thr1392Met | |
| NM_001354904.2:c.4100C>T | NP_001341833.1:p.Thr1367Met | |
| NM_001354905.2:c.3998C>T | NP_001341834.1:p.Thr1333Met | |
| NM_001354906.2:c.3629C>T | NP_001341835.1:p.Thr1210Met |