Linked Data
ClinVar Variation Id:
540036
dbSNP Id:
rs373532334
ExAC:
14:105177987 G / A
gnomAD v2:
14-105177987-G-A
gnomAD v3:
14-104711650-G-A
gnomAD v4:
14-104711650-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.104711650G>A , CM000676.2:g.104711650G>A | GRCh38 |
| NC_000014.8:g.105177987G>A , CM000676.1:g.105177987G>A | GRCh37 |
| NC_000014.7:g.104249032G>A | NCBI36 |
| NG_027684.1:g.27045G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392634.9:c.2440G>A MANE Select | ENSP00000376410.4:p.Asp814Asn | |
| ENST00000617571.5:c.2440G>A | ENSP00000483829.2:p.Asp814Asn | |
| ENST00000674520.1:c.2440G>A | ENSP00000502593.1:p.Asp814Asn | |
| ENST00000674631.1:c.478G>A | ENSP00000502830.1:p.Asp160Asn | |
| ENST00000674662.1:c.2444G>A | ENSP00000501895.1:n.2444G>A | |
| ENST00000674757.1:c.2440G>A | ENSP00000502202.1:p.Asp814Asn | |
| ENST00000674822.1:c.2324G>A | ENSP00000501552.1:n.2324G>A | |
| ENST00000674846.1:c.2435G>A | ENSP00000502431.1:n.2435G>A | |
| ENST00000674857.1:c.2429G>A | ENSP00000501687.1:n.2429G>A | |
| ENST00000674960.1:c.2298G>A | ENSP00000501841.1:n.2298G>A | |
| ENST00000674991.1:c.1690G>A | ENSP00000502004.1:p.Asp564Asn | |
| ENST00000674994.1:c.2406G>A | ENSP00000502442.1:n.2406G>A | |
| ENST00000675207.1:c.2536G>A | ENSP00000502644.1:p.Asp846Asn | |
| ENST00000675329.1:c.2416G>A | ENSP00000502287.1:p.Asp806Asn | |
| ENST00000675481.1:c.2440G>A | ENSP00000502723.1:p.Asp814Asn | |
| ENST00000675557.1:n.219G>A | ||
| ENST00000675583.1:c.2369G>A | ENSP00000501740.1:n.2369G>A | |
| ENST00000675638.1:c.2440G>A | ENSP00000501647.1:p.Asp814Asn | |
| ENST00000675724.1:c.2378G>A | ENSP00000502576.1:n.2378G>A | |
| ENST00000675771.1:c.1703G>A | ENSP00000502104.1:n.1703G>A | |
| ENST00000675797.1:c.1845G>A | ENSP00000502023.1:n.1845G>A | |
| ENST00000675809.1:c.2495G>A | ENSP00000502587.1:n.2495G>A | |
| ENST00000675930.1:c.2440G>A | ENSP00000502456.1:p.Asp814Asn | |
| ENST00000675980.1:c.2458G>A | ENSP00000502520.1:p.Asp820Asn | |
| ENST00000676016.1:c.2339G>A | ENSP00000502412.1:n.2339G>A | |
| ENST00000676366.1:c.2440G>A | ENSP00000501605.1:p.Asp814Asn | |
| ENST00000252527.8:c.844G>A | ENSP00000252527.8:p.Asp282Asn | |
| ENST00000330634.11:c.2440G>A | ENSP00000376406.3:p.Asp814Asn | |
| ENST00000392634.8:c.2440G>A | ENSP00000376410.4:p.Asp814Asn | |
| ENST00000474229.1:n.933G>A | ||
| ENST00000480763.2:n.305G>A | ||
| ENST00000617571.4:c.-1694G>A | ENSP00000483829.1:n.-1694G>A | |
| NM_001031714.3:c.2440G>A | NP_001026884.3:p.Asp814Asn | |
| NM_022489.3:c.2440G>A | NP_071934.3:p.Asp814Asn | |
| XM_005268004.3:c.2536G>A | XP_005268061.1:p.Asp846Asn | |
| XM_005268005.3:c.2536G>A | XP_005268062.1:p.Asp846Asn | |
| XR_943507.1:n.2665G>A | ||
| XM_005268004.4:c.2536G>A | XP_005268061.1:p.Asp846Asn | |
| XM_005268005.4:c.2536G>A | XP_005268062.1:p.Asp846Asn | |
| XM_017021595.1:c.2536G>A | XP_016877084.1:p.Asp846Asn | |
| XR_001750518.1:n.2696G>A | ||
| NM_001031714.4:c.2440G>A | NP_001026884.3:p.Asp814Asn | |
| NM_022489.4:c.2440G>A MANE Select | NP_071934.3:p.Asp814Asn |