Linked Data
ClinVar Variation Id:
51681
dbSNP Id:
rs397507731
ExAC:
13:32913079 G / GA
gnomAD v2:
13-32913079-G-GA
gnomAD v4:
13-32338942-G-GA
MyVariant Identifiers:
chr13:g.32913085dupA (hg19)
chr13:g.32913079_32913080insA (hg19)
chr13:g.32338948dupA (hg38)
chr13:g.32338942_32338943insA (hg38)
PubMed:
PMID:11802209
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32338948dup , CM000675.2:g.32338948dup | GRCh38 |
| NC_000013.10:g.32913085dup , CM000675.1:g.32913085dup | GRCh37 |
| NC_000013.9:g.31811085dup | NCBI36 |
| NG_012772.3:g.28469dup , LRG_293:g.28469dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.4593dup | ENSP00000434898.2:p.Val1532SerfsTer2 | |
| ENST00000528762.2:c.4593dup | ENSP00000433168.2:p.Val1532SerfsTer2 | |
| ENST00000530893.7:c.4224dup | ENSP00000499438.2:p.Val1409SerfsTer2 | |
| ENST00000665585.2:c.4593dup | ENSP00000499570.2:p.Val1532SerfsTer2 | |
| ENST00000666593.2:c.4593dup | ENSP00000499256.2:p.Val1532SerfsTer2 | |
| ENST00000700202.2:c.4593dup | ENSP00000514856.2:p.Val1532SerfsTer2 | |
| ENST00000380152.8:c.4593dup MANE Select | ENSP00000369497.3:p.Val1532SerfsTer2 | |
| ENST00000544455.6:c.4593dup | ENSP00000439902.1:p.Val1532SerfsTer2 | |
| ENST00000614259.2:c.4593dup | ENSP00000506251.1:p.Val1532SerfsTer2 | |
| ENST00000680887.1:c.4593dup | ENSP00000505508.1:p.Val1532SerfsTer2 | |
| ENST00000380152.7:c.4593dup | ENSP00000369497.3:p.Val1532SerfsTer2 | |
| ENST00000544455.5:c.4593dup | ENSP00000439902.1:p.Val1532SerfsTer2 | |
| ENST00000614259.1:n.4593dup | ||
| NM_000059.3:c.4593dup , LRG_293t1:c.4593dup | NP_000050.2:p.Val1532SerfsTer2 | |
| XM_011535203.1:c.4593dup | XP_011533505.1:p.Val1532SerfsTer2 | |
| XM_011535204.1:c.4593dup | XP_011533506.1:p.Val1532SerfsTer2 | |
| XM_011535205.1:c.4593dup | XP_011533507.1:p.Val1532SerfsTer2 | |
| NM_000059.4:c.4593dup MANE Select | NP_000050.3:p.Val1532SerfsTer2 |