Linked Data
ClinVar Variation Id:
142885
dbSNP Id:
rs587782795
ExAC:
13:32900240 C / G
gnomAD v2:
13-32900240-C-G
gnomAD v3:
13-32326103-C-G
gnomAD v4:
13-32326103-C-G
MyVariant Identifiers:
chr13:g.32900240C>G (hg19)
chr13:g.32900240_32900243delinsGTGT (hg19)
chr13:g.32326103C>G (hg38)
chr13:g.32326103_32326106delinsGTGT (hg38)
PubMed:
PMID:26295337
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32326103C>G , CM000675.2:g.32326103C>G | GRCh38 |
| NC_000013.10:g.32900240C>G , CM000675.1:g.32900240C>G | GRCh37 |
| NC_000013.9:g.31798240C>G | NCBI36 |
| NG_012772.3:g.15624C>G , LRG_293:g.15624C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.428C>G | ENSP00000434898.2:p.Pro143Arg | |
| ENST00000528762.2:c.428C>G | ENSP00000433168.2:p.Pro143Arg | |
| ENST00000530893.7:c.59C>G | ENSP00000499438.2:p.Pro20Arg | |
| ENST00000665585.2:c.428C>G | ENSP00000499570.2:p.Pro143Arg | |
| ENST00000666593.2:c.428C>G | ENSP00000499256.2:p.Pro143Arg | |
| ENST00000700202.2:c.428C>G | ENSP00000514856.2:p.Pro143Arg | |
| ENST00000700200.1:n.299C>G | ||
| ENST00000700201.1:c.*207C>G | ENSP00000514855.1:n.*207C>G | |
| ENST00000380152.8:c.428C>G MANE Select | ENSP00000369497.3:p.Pro143Arg | |
| ENST00000544455.6:c.428C>G | ENSP00000439902.1:p.Pro143Arg | |
| ENST00000614259.2:c.428C>G | ENSP00000506251.1:p.Pro143Arg | |
| ENST00000680887.1:c.428C>G | ENSP00000505508.1:p.Pro143Arg | |
| ENST00000380152.7:c.428C>G | ENSP00000369497.3:p.Pro143Arg | |
| ENST00000530893.6:n.626C>G | ||
| ENST00000544455.5:c.428C>G | ENSP00000439902.1:p.Pro143Arg | |
| ENST00000614259.1:n.428C>G | ||
| NM_000059.3:c.428C>G , LRG_293t1:c.428C>G | NP_000050.2:p.Pro143Arg | |
| XM_011535203.1:c.428C>G | XP_011533505.1:p.Pro143Arg | |
| XM_011535204.1:c.428C>G | XP_011533506.1:p.Pro143Arg | |
| XM_011535205.1:c.428C>G | XP_011533507.1:p.Pro143Arg | |
| NM_000059.4:c.428C>G MANE Select | NP_000050.3:p.Pro143Arg |