Linked Data
ClinVar Variation Id:
96762
ClinVar RCV Id:
RCV000082883
RCV000129740
RCV000197010
RCV000294429
RCV000587492
RCV000677855
RCV001353634
RCV003493437
dbSNP Id:
rs397507263
ExAC:
13:32906781 C / A
gnomAD v2:
13-32906781-C-A
gnomAD v3:
13-32332644-C-A
gnomAD v4:
13-32332644-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32332644C>A , CM000675.2:g.32332644C>A | GRCh38 |
| NC_000013.10:g.32906781C>A , CM000675.1:g.32906781C>A | GRCh37 |
| NC_000013.9:g.31804781C>A | NCBI36 |
| NG_012772.3:g.22165C>A , LRG_293:g.22165C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.1166C>A | ENSP00000434898.2:p.Pro389Gln | |
| ENST00000528762.2:c.1166C>A | ENSP00000433168.2:p.Pro389Gln | |
| ENST00000530893.7:c.797C>A | ENSP00000499438.2:p.Pro266Gln | |
| ENST00000665585.2:c.1166C>A | ENSP00000499570.2:p.Pro389Gln | |
| ENST00000666593.2:c.1166C>A | ENSP00000499256.2:p.Pro389Gln | |
| ENST00000700202.2:c.1166C>A | ENSP00000514856.2:p.Pro389Gln | |
| ENST00000700201.1:c.*945C>A | ENSP00000514855.1:n.*945C>A | |
| ENST00000380152.8:c.1166C>A MANE Select | ENSP00000369497.3:p.Pro389Gln | |
| ENST00000544455.6:c.1166C>A | ENSP00000439902.1:p.Pro389Gln | |
| ENST00000614259.2:c.1166C>A | ENSP00000506251.1:p.Pro389Gln | |
| ENST00000680887.1:c.1166C>A | ENSP00000505508.1:p.Pro389Gln | |
| ENST00000380152.7:c.1166C>A | ENSP00000369497.3:p.Pro389Gln | |
| ENST00000530893.6:n.1364C>A | ||
| ENST00000544455.5:c.1166C>A | ENSP00000439902.1:p.Pro389Gln | |
| ENST00000614259.1:n.1166C>A | ||
| NM_000059.3:c.1166C>A , LRG_293t1:c.1166C>A | NP_000050.2:p.Pro389Gln | |
| XM_011535203.1:c.1166C>A | XP_011533505.1:p.Pro389Gln | |
| XM_011535204.1:c.1166C>A | XP_011533506.1:p.Pro389Gln | |
| XM_011535205.1:c.1166C>A | XP_011533507.1:p.Pro389Gln | |
| NM_000059.4:c.1166C>A MANE Select | NP_000050.3:p.Pro389Gln |