Linked Data
ClinVar Variation Id:
225122
dbSNP Id:
rs879255594
gnomAD v4:
3-193643436-G-A
PubMed:
PMID:25012220
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.193643436G>A , CM000665.2:g.193643436G>A | GRCh38 |
| NC_000003.11:g.193361225G>A , CM000665.1:g.193361225G>A | GRCh37 |
| NC_000003.10:g.194843919G>A | NCBI36 |
| NG_011605.1:g.55293G>A , LRG_337:g.55293G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361510.8:c.1369G>A MANE Select | ENSP00000355324.2:p.Val457Met | |
| ENST00000361828.7:c.1204G>A | ENSP00000354429.3:p.Val402Met | |
| ENST00000361908.8:c.1315G>A | ENSP00000354681.3:p.Val439Met | |
| ENST00000392436.7:c.1204G>A | ENSP00000376231.3:p.Val402Met | |
| ENST00000392437.6:c.1258G>A | ENSP00000376232.2:p.Val420Met | |
| ENST00000642289.1:c.1143G>A | ||
| ENST00000642445.1:c.1204G>A | ENSP00000495535.1:p.Val402Met | |
| ENST00000642593.1:c.1204G>A | ENSP00000494273.1:p.Val402Met | |
| ENST00000643329.1:c.886G>A | ENSP00000493673.1:p.Val296Met | |
| ENST00000643737.1:c.*1285G>A | ENSP00000494210.1:n.*1285G>A | |
| ENST00000644595.1:c.1204G>A | ENSP00000494121.1:p.Val402Met | |
| ENST00000644629.1:c.864G>A | ||
| ENST00000644841.1:c.832G>A | ENSP00000493988.1:p.Val278Met | |
| ENST00000644959.1:c.1173G>A | ||
| ENST00000645553.1:c.1219G>A | ENSP00000494725.1:p.Val407Met | |
| ENST00000646085.1:c.*682G>A | ENSP00000494509.1:n.*682G>A | |
| ENST00000646277.1:c.1369G>A | ENSP00000495289.1:p.Val457Met | |
| ENST00000646544.1:c.192G>A | ||
| ENST00000646699.1:c.1143G>A | ||
| ENST00000646793.1:c.1096G>A | ENSP00000494512.1:p.Val366Met | |
| ENST00000361150.6:c.1207G>A | ENSP00000354781.2:p.Val403Met | |
| ENST00000361510.6:c.1369G>A | ENSP00000355324.2:p.Val457Met | |
| ENST00000361715.6:c.1261G>A | ENSP00000355311.2:p.Val421Met | |
| ENST00000361828.6:c.1258G>A | ENSP00000354429.2:p.Val420Met | |
| ENST00000361908.7:c.1315G>A | ENSP00000354681.3:p.Val439Met | |
| ENST00000392438.7:c.1204G>A | ENSP00000376233.3:p.Val402Met | |
| ENST00000475899.1:n.400G>A | ||
| NM_015560.2:c.1204G>A , LRG_337t1:c.1204G>A | NP_056375.2:p.Val402Met | |
| NM_130831.2:c.1096G>A | NP_570844.1:p.Val366Met | |
| NM_130832.2:c.1150G>A | NP_570845.1:p.Val384Met | |
| NM_130833.2:c.1207G>A | NP_570846.1:p.Val403Met | |
| NM_130834.2:c.1258G>A | NP_570847.2:p.Val420Met | |
| NM_130835.2:c.1261G>A | NP_570848.1:p.Val421Met | |
| NM_130836.2:c.1315G>A | NP_570849.2:p.Val439Met | |
| NM_130837.2:c.1369G>A , LRG_337t2:c.1369G>A | NP_570850.2:p.Val457Met | |
| XM_011512863.1:c.1369G>A | XP_011511165.1:p.Val457Met | |
| XM_011512864.1:c.1315G>A | XP_011511166.1:p.Val439Met | |
| XM_011512865.1:c.1258G>A | XP_011511167.1:p.Val420Met | |
| XM_011512866.1:c.1207G>A | XP_011511168.1:p.Val403Met | |
| XM_011512867.1:c.1204G>A | XP_011511169.1:p.Val402Met | |
| XM_011512868.1:c.1096G>A | XP_011511170.1:p.Val366Met | |
| XM_011512869.1:c.1369G>A | XP_011511171.1:p.Val457Met | |
| NM_001354663.1:c.835G>A | NP_001341592.1:p.Val279Met | |
| NM_001354664.1:c.832G>A | NP_001341593.1:p.Val278Met | |
| XR_001740158.2:n.1598G>A | ||
| XR_001740159.2:n.1433G>A | ||
| NM_001354663.2:c.835G>A | NP_001341592.1:p.Val279Met | |
| NM_001354664.2:c.832G>A | NP_001341593.1:p.Val278Met | |
| NM_130831.3:c.1096G>A | NP_570844.1:p.Val366Met | |
| NM_130832.3:c.1150G>A | NP_570845.1:p.Val384Met | |
| NM_130834.3:c.1258G>A | NP_570847.2:p.Val420Met | |
| NM_130836.3:c.1315G>A | NP_570849.2:p.Val439Met | |
| NM_015560.3:c.1204G>A | NP_056375.2:p.Val402Met | |
| NM_130833.3:c.1207G>A | NP_570846.1:p.Val403Met | |
| NM_130835.3:c.1261G>A | NP_570848.1:p.Val421Met | |
| NM_130837.3:c.1369G>A MANE Select | NP_570850.2:p.Val457Met |