Linked Data
ClinVar Variation Id:
540041
dbSNP Id:
rs370719592
ExAC:
14:105179892 G / A
gnomAD v2:
14-105179892-G-A
gnomAD v3:
14-104713555-G-A
gnomAD v4:
14-104713555-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.104713555G>A , CM000676.2:g.104713555G>A | GRCh38 |
| NC_000014.8:g.105179892G>A , CM000676.1:g.105179892G>A | GRCh37 |
| NC_000014.7:g.104250937G>A | NCBI36 |
| NG_027684.1:g.28950G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392634.9:c.2989G>A MANE Select | ENSP00000376410.4:p.Asp997Asn | |
| ENST00000617571.5:c.2985G>A | ENSP00000483829.2:p.Pro995= | |
| ENST00000674520.1:c.2984G>A | ENSP00000502593.1:n.2984G>A | |
| ENST00000674631.1:c.1027G>A | ENSP00000502830.1:p.Asp343Asn | |
| ENST00000674662.1:c.2993G>A | ENSP00000501895.1:n.2993G>A | |
| ENST00000674757.1:c.2994G>A | ENSP00000502202.1:p.Pro998= | |
| ENST00000674822.1:c.2873G>A | ENSP00000501552.1:n.2873G>A | |
| ENST00000674846.1:c.2984G>A | ENSP00000502431.1:n.2984G>A | |
| ENST00000674857.1:c.2978G>A | ENSP00000501687.1:n.2978G>A | |
| ENST00000674960.1:c.2847G>A | ENSP00000501841.1:n.2847G>A | |
| ENST00000674991.1:c.2239G>A | ENSP00000502004.1:p.Asp747Asn | |
| ENST00000674994.1:c.2955G>A | ENSP00000502442.1:n.2955G>A | |
| ENST00000675207.1:c.3085G>A | ENSP00000502644.1:p.Asp1029Asn | |
| ENST00000675329.1:c.2965G>A | ENSP00000502287.1:p.Asp989Asn | |
| ENST00000675481.1:c.2989G>A | ENSP00000502723.1:p.Asp997Asn | |
| ENST00000675583.1:c.2918G>A | ENSP00000501740.1:n.2918G>A | |
| ENST00000675603.1:n.116G>A | ||
| ENST00000675638.1:c.2989G>A | ENSP00000501647.1:p.Asp997Asn | |
| ENST00000675724.1:c.2927G>A | ENSP00000502576.1:n.2927G>A | |
| ENST00000675771.1:c.2252G>A | ENSP00000502104.1:n.2252G>A | |
| ENST00000675797.1:c.2394G>A | ENSP00000502023.1:n.2394G>A | |
| ENST00000675809.1:c.3044G>A | ENSP00000502587.1:n.3044G>A | |
| ENST00000675930.1:c.2989G>A | ENSP00000502456.1:p.Asp997Asn | |
| ENST00000675980.1:c.3007G>A | ENSP00000502520.1:p.Asp1003Asn | |
| ENST00000676016.1:c.2888G>A | ENSP00000502412.1:n.2888G>A | |
| ENST00000676366.1:c.2989G>A | ENSP00000501605.1:p.Asp997Asn | |
| ENST00000252527.8:c.1393G>A | ENSP00000252527.8:p.Asp465Asn | |
| ENST00000330634.11:c.2989G>A | ENSP00000376406.3:p.Asp997Asn | |
| ENST00000392634.8:c.2989G>A | ENSP00000376410.4:p.Asp997Asn | |
| ENST00000477497.1:n.494G>A | ||
| ENST00000617571.4:c.-1145G>A | ENSP00000483829.1:n.-1145G>A | |
| NM_001031714.3:c.2989G>A | NP_001026884.3:p.Asp997Asn | |
| NM_022489.3:c.2989G>A | NP_071934.3:p.Asp997Asn | |
| XM_005268004.3:c.3085G>A | XP_005268061.1:p.Asp1029Asn | |
| XM_005268005.3:c.3085G>A | XP_005268062.1:p.Asp1029Asn | |
| XR_943507.1:n.3214G>A | ||
| XM_005268004.4:c.3085G>A | XP_005268061.1:p.Asp1029Asn | |
| XM_005268005.4:c.3085G>A | XP_005268062.1:p.Asp1029Asn | |
| XM_017021595.1:c.3085G>A | XP_016877084.1:p.Asp1029Asn | |
| NM_001031714.4:c.2989G>A | NP_001026884.3:p.Asp997Asn | |
| NM_022489.4:c.2989G>A MANE Select | NP_071934.3:p.Asp997Asn |