Linked Data
ClinVar Variation Id:
133525
dbSNP Id:
rs564314108
ExAC:
5:112174298 G / A
gnomAD v2:
5-112174298-G-A
gnomAD v3:
5-112838601-G-A
gnomAD v4:
5-112838601-G-A
COSMIC:
COSM1162555
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838601G>A , CM000667.2:g.112838601G>A | GRCh38 |
| NC_000005.9:g.112174298G>A , CM000667.1:g.112174298G>A | GRCh37 |
| NC_000005.8:g.112202197G>A | NCBI36 |
| NG_008481.4:g.151081G>A , LRG_130:g.151081G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2672G>A | ENSP00000484935.2:n.2672G>A | |
| ENST00000504915.3:c.3061G>A | ENSP00000473355.2:p.Asp1021Asn | |
| ENST00000505350.2:c.*3013G>A | ENSP00000481752.1:n.*3013G>A | |
| ENST00000507379.6:c.2953G>A | ENSP00000423224.2:p.Asp985Asn | |
| ENST00000509732.6:c.3007G>A | ENSP00000426541.2:p.Asp1003Asn | |
| ENST00000512211.7:c.3007G>A | ENSP00000423828.3:p.Asp1003Asn | |
| ENST00000257430.9:c.3007G>A MANE Select | ENSP00000257430.4:p.Asp1003Asn | |
| ENST00000257430.8:c.3007G>A | ENSP00000257430.4:p.Asp1003Asn | |
| ENST00000502371.2:c.1360G>A | ||
| ENST00000507379.5:c.2953G>A | ENSP00000423224.1:p.Asp985Asn | |
| ENST00000508376.6:c.3007G>A | ENSP00000427089.2:p.Asp1003Asn | |
| ENST00000508624.5:c.*2329G>A | ENSP00000424265.1:n.*2329G>A | |
| ENST00000512211.6:c.3007G>A | ENSP00000423828.2:p.Asp1003Asn | |
| ENST00000520401.1:c.230+9629G>A | ||
| NM_000038.5:c.3007G>A | NP_000029.2:p.Asp1003Asn | |
| NM_001127510.2:c.3007G>A | NP_001120982.1:p.Asp1003Asn | |
| NM_001127511.2:c.2953G>A | NP_001120983.2:p.Asp985Asn | |
| NM_001354895.1:c.3007G>A | NP_001341824.1:p.Asp1003Asn | |
| NM_001354896.1:c.3061G>A | NP_001341825.1:p.Asp1021Asn | |
| NM_001354897.1:c.3037G>A | NP_001341826.1:p.Asp1013Asn | |
| NM_001354898.1:c.2932G>A | NP_001341827.1:p.Asp978Asn | |
| NM_001354899.1:c.2923G>A | NP_001341828.1:p.Asp975Asn | |
| NM_001354900.1:c.2884G>A | NP_001341829.1:p.Asp962Asn | |
| NM_001354901.1:c.2830G>A | NP_001341830.1:p.Asp944Asn | |
| NM_001354902.1:c.2734G>A | NP_001341831.1:p.Asp912Asn | |
| NM_001354903.1:c.2704G>A | NP_001341832.1:p.Asp902Asn | |
| NM_001354904.1:c.2629G>A | NP_001341833.1:p.Asp877Asn | |
| NM_001354905.1:c.2527G>A | NP_001341834.1:p.Asp843Asn | |
| NM_001354906.1:c.2158G>A | NP_001341835.1:p.Asp720Asn | |
| NM_000038.6:c.3007G>A MANE Select | NP_000029.2:p.Asp1003Asn | |
| NM_001127510.3:c.3007G>A | NP_001120982.1:p.Asp1003Asn | |
| NM_001127511.3:c.2953G>A | NP_001120983.2:p.Asp985Asn | |
| NM_001354895.2:c.3007G>A | NP_001341824.1:p.Asp1003Asn | |
| NM_001354896.2:c.3061G>A | NP_001341825.1:p.Asp1021Asn | |
| NM_001354897.2:c.3037G>A | NP_001341826.1:p.Asp1013Asn | |
| NM_001354898.2:c.2932G>A | NP_001341827.1:p.Asp978Asn | |
| NM_001354899.2:c.2923G>A | NP_001341828.1:p.Asp975Asn | |
| NM_001354900.2:c.2884G>A | NP_001341829.1:p.Asp962Asn | |
| NM_001354901.2:c.2830G>A | NP_001341830.1:p.Asp944Asn | |
| NM_001354902.2:c.2734G>A | NP_001341831.1:p.Asp912Asn | |
| NM_001354903.2:c.2704G>A | NP_001341832.1:p.Asp902Asn | |
| NM_001354904.2:c.2629G>A | NP_001341833.1:p.Asp877Asn | |
| NM_001354905.2:c.2527G>A | NP_001341834.1:p.Asp843Asn | |
| NM_001354906.2:c.2158G>A | NP_001341835.1:p.Asp720Asn |