Linked Data
ClinVar Variation Id:
531350
dbSNP Id:
rs1334767632
gnomAD v2:
13-32906574-T-C
gnomAD v3:
13-32332437-T-C
gnomAD v4:
13-32332437-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32332437T>C , CM000675.2:g.32332437T>C | GRCh38 |
| NC_000013.10:g.32906574T>C , CM000675.1:g.32906574T>C | GRCh37 |
| NC_000013.9:g.31804574T>C | NCBI36 |
| NG_012772.3:g.21958T>C , LRG_293:g.21958T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.959T>C | ENSP00000434898.2:p.Leu320Pro | |
| ENST00000528762.2:c.959T>C | ENSP00000433168.2:p.Leu320Pro | |
| ENST00000530893.7:c.590T>C | ENSP00000499438.2:p.Leu197Pro | |
| ENST00000665585.2:c.959T>C | ENSP00000499570.2:p.Leu320Pro | |
| ENST00000666593.2:c.959T>C | ENSP00000499256.2:p.Leu320Pro | |
| ENST00000700202.2:c.959T>C | ENSP00000514856.2:p.Leu320Pro | |
| ENST00000700201.1:c.*738T>C | ENSP00000514855.1:n.*738T>C | |
| ENST00000380152.8:c.959T>C MANE Select | ENSP00000369497.3:p.Leu320Pro | |
| ENST00000544455.6:c.959T>C | ENSP00000439902.1:p.Leu320Pro | |
| ENST00000614259.2:c.959T>C | ENSP00000506251.1:p.Leu320Pro | |
| ENST00000680887.1:c.959T>C | ENSP00000505508.1:p.Leu320Pro | |
| ENST00000380152.7:c.959T>C | ENSP00000369497.3:p.Leu320Pro | |
| ENST00000530893.6:n.1157T>C | ||
| ENST00000544455.5:c.959T>C | ENSP00000439902.1:p.Leu320Pro | |
| ENST00000614259.1:n.959T>C | ||
| NM_000059.3:c.959T>C , LRG_293t1:c.959T>C | NP_000050.2:p.Leu320Pro | |
| XM_011535203.1:c.959T>C | XP_011533505.1:p.Leu320Pro | |
| XM_011535204.1:c.959T>C | XP_011533506.1:p.Leu320Pro | |
| XM_011535205.1:c.959T>C | XP_011533507.1:p.Leu320Pro | |
| NM_000059.4:c.959T>C MANE Select | NP_000050.3:p.Leu320Pro |