Linked Data
dbSNP Id:
rs775892050
gnomAD v2:
13-32931851-C-CT
gnomAD v4:
13-32357714-C-CT
MyVariant Identifiers:
chr13:g.32931852_32931853insT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32357720dup , CM000675.2:g.32357720dup | GRCh38 |
| NC_000013.10:g.32931857dup , CM000675.1:g.32931857dup | GRCh37 |
| NC_000013.9:g.31829857dup | NCBI36 |
| NG_012772.3:g.47241dup , LRG_293:g.47241dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.7618-22dup | ENSP00000434898.2:n.7618-22dup | |
| ENST00000528762.2:c.7618-22dup | ENSP00000433168.2:n.7618-22dup | |
| ENST00000530893.7:c.7249-22dup | ENSP00000499438.2:n.7249-22dup | |
| ENST00000665585.2:c.7618-22dup | ENSP00000499570.2:n.7618-22dup | |
| ENST00000666593.2:c.7618-22dup | ENSP00000499256.2:n.7618-22dup | |
| ENST00000700202.2:c.7618-22dup | ENSP00000514856.2:n.7618-22dup | |
| ENST00000700202.1:c.85-22dup | ENSP00000514856.1:n.85-22dup | |
| ENST00000380152.8:c.7618-22dup MANE Select | ENSP00000369497.3:n.7618-22dup | |
| ENST00000544455.6:c.7618-22dup | ENSP00000439902.1:n.7618-22dup | |
| ENST00000614259.2:c.7618-22dup | ENSP00000506251.1:n.7618-22dup | |
| ENST00000665585.1:c.183-22dup | ||
| ENST00000680887.1:c.7618-22dup | ENSP00000505508.1:n.7618-22dup | |
| ENST00000380152.7:c.7618-22dup | ENSP00000369497.3:n.7618-22dup | |
| ENST00000544455.5:c.7618-22dup | ENSP00000439902.1:n.7618-22dup | |
| ENST00000614259.1:n.7618-22dup | ||
| NM_000059.3:c.7618-22dup , LRG_293t1:c.7618-22dup | NP_000050.2:n.7618-22dup | |
| XM_011535203.1:c.7618-22dup | XP_011533505.1:n.7618-22dup | |
| XM_011535204.1:c.7522-22dup | XP_011533506.1:n.7522-22dup | |
| XM_011535205.1:c.7618-22dup | XP_011533507.1:n.7618-22dup | |
| NM_000059.4:c.7618-22dup MANE Select | NP_000050.3:n.7618-22dup |