Linked Data
ClinVar Variation Id:
52434
dbSNP Id:
rs80359017
gnomAD v4:
13-32362632-C-G
PubMed:
PMID:19043619
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32362632C>G , CM000675.2:g.32362632C>G | GRCh38 |
| NC_000013.10:g.32936769C>G , CM000675.1:g.32936769C>G | GRCh37 |
| NC_000013.9:g.31834769C>G | NCBI36 |
| NG_012772.3:g.52153C>G , LRG_293:g.52153C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.7915C>G | ENSP00000434898.2:p.Pro2639Ala | |
| ENST00000528762.2:c.7915C>G | ENSP00000433168.2:p.Pro2639Ala | |
| ENST00000530893.7:c.7546C>G | ENSP00000499438.2:p.Pro2516Ala | |
| ENST00000665585.2:c.7915C>G | ENSP00000499570.2:p.Pro2639Ala | |
| ENST00000666593.2:c.7915C>G | ENSP00000499256.2:p.Pro2639Ala | |
| ENST00000700202.2:c.7915C>G | ENSP00000514856.2:p.Pro2639Ala | |
| ENST00000700202.1:c.382C>G | ENSP00000514856.1:p.Pro128Ala | |
| ENST00000380152.8:c.7915C>G MANE Select | ENSP00000369497.3:p.Pro2639Ala | |
| ENST00000544455.6:c.7915C>G | ENSP00000439902.1:p.Pro2639Ala | |
| ENST00000614259.2:c.7923C>G | ENSP00000506251.1:p.Phe2641Leu | |
| ENST00000665585.1:c.480C>G | ||
| ENST00000680887.1:c.7915C>G | ENSP00000505508.1:p.Pro2639Ala | |
| ENST00000380152.7:c.7915C>G | ENSP00000369497.3:p.Pro2639Ala | |
| ENST00000544455.5:c.7915C>G | ENSP00000439902.1:p.Pro2639Ala | |
| ENST00000614259.1:n.7923C>G | ||
| NM_000059.3:c.7915C>G , LRG_293t1:c.7915C>G | NP_000050.2:p.Pro2639Ala | |
| XM_011535203.1:c.7915C>G | XP_011533505.1:p.Pro2639Ala | |
| XM_011535204.1:c.7819C>G | XP_011533506.1:p.Pro2607Ala | |
| XM_011535205.1:c.7915C>G | XP_011533507.1:p.Pro2639Ala | |
| NM_000059.4:c.7915C>G MANE Select | NP_000050.3:p.Pro2639Ala |