Linked Data
ClinVar Variation Id:
425054
dbSNP Id:
rs1034508175
gnomAD v2:
14-102449797-G-A
gnomAD v3:
14-101983460-G-A
gnomAD v4:
14-101983460-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.101983460G>A , CM000676.2:g.101983460G>A | GRCh38 |
| NC_000014.8:g.102449797G>A , CM000676.1:g.102449797G>A | GRCh37 |
| NC_000014.7:g.101519550G>A | NCBI36 |
| NG_008777.1:g.23933G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684561.1:c.1312G>A | ENSP00000506816.1:p.Val438Ile | |
| ENST00000360184.10:c.1312G>A MANE Select | ENSP00000348965.4:p.Val438Ile | |
| ENST00000643508.2:c.1312G>A | ENSP00000495528.2:p.Val438Ile | |
| ENST00000643684.1:n.1431G>A | ||
| ENST00000643958.2:c.1312G>A | ENSP00000505734.1:p.Val438Ile | |
| ENST00000644881.2:c.1312G>A | ENSP00000495022.2:p.Val438Ile | |
| ENST00000645039.2:c.1312G>A | ENSP00000495220.2:p.Val438Ile | |
| ENST00000645114.2:c.1312G>A | ENSP00000495884.2:p.Val438Ile | |
| ENST00000645149.2:c.1312G>A | ENSP00000495944.2:p.Val438Ile | |
| ENST00000679486.1:c.1312G>A | ENSP00000506688.1:p.Val438Ile | |
| ENST00000679629.1:c.1312G>A | ENSP00000505589.1:p.Val438Ile | |
| ENST00000679720.1:c.1312G>A | ENSP00000505938.1:p.Val438Ile | |
| ENST00000679910.1:c.1312G>A | ENSP00000506521.1:p.Val438Ile | |
| ENST00000680001.1:c.*821G>A | ENSP00000506351.1:n.*821G>A | |
| ENST00000680120.1:c.1312G>A | ENSP00000504863.1:p.Val438Ile | |
| ENST00000680137.1:c.1312G>A | ENSP00000505294.1:p.Val438Ile | |
| ENST00000680200.1:c.1312G>A | ENSP00000506166.1:p.Val438Ile | |
| ENST00000680313.1:c.1312G>A | ENSP00000506208.1:p.Val438Ile | |
| ENST00000680423.1:c.1312G>A | ENSP00000505483.1:p.Val438Ile | |
| ENST00000680715.1:c.1312G>A | ENSP00000505332.1:p.Val438Ile | |
| ENST00000680808.1:c.1312G>A | ENSP00000506446.1:p.Val438Ile | |
| ENST00000680874.1:c.1312G>A | ENSP00000504911.1:p.Val438Ile | |
| ENST00000681010.1:c.1312G>A | ENSP00000505201.1:p.Val438Ile | |
| ENST00000681066.1:c.1312G>A | ENSP00000506344.1:p.Val438Ile | |
| ENST00000681123.1:c.1312G>A | ENSP00000506124.1:p.Val438Ile | |
| ENST00000681283.1:c.1312G>A | ENSP00000505667.1:p.Val438Ile | |
| ENST00000681311.1:c.1312G>A | ENSP00000505519.1:p.Val438Ile | |
| ENST00000681536.1:c.1312G>A | ENSP00000505821.1:p.Val438Ile | |
| ENST00000681574.1:c.1312G>A | ENSP00000505523.1:p.Val438Ile | |
| ENST00000681668.1:c.1312G>A | ENSP00000506420.1:p.Val438Ile | |
| ENST00000681751.1:c.*1043G>A | ENSP00000506637.1:n.*1043G>A | |
| ENST00000681822.1:c.1312G>A | ENSP00000505744.1:p.Val438Ile | |
| ENST00000681859.1:c.1312G>A | ENSP00000505467.1:p.Val438Ile | |
| ENST00000360184.8:c.1312G>A | ENSP00000348965.4:p.Val438Ile | |
| NM_001376.4:c.1312G>A | NP_001367.2:p.Val438Ile | |
| NM_001376.5:c.1312G>A MANE Select | NP_001367.2:p.Val438Ile |