Linked Data
ClinVar Variation Id:
860109
ClinVar RCV Id:
RCV001066360
dbSNP Id:
rs1853449457
gnomAD v4:
11-32434938-A-AGGCGGCGGCGGCGGGGGT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.32434947_32434964dup , CM000673.2:g.32434947_32434964dup | GRCh38 |
| NC_000011.9:g.32456493_32456510dup , CM000673.1:g.32456493_32456510dup | GRCh37 |
| NC_000011.8:g.32413069_32413086dup | NCBI36 |
| NG_009272.1:g.5586_5603dup , LRG_525:g.5586_5603dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332351.9:c.405_422dup | ENSP00000331327.5:p.Pro141_His142insProProProProProPro | |
| ENST00000379077.9:c.405_422dup | ENSP00000368368.5:p.Pro141_His142insProProProProProPro | |
| ENST00000448076.9:c.405_422dup | ENSP00000413452.5:p.Pro141_His142insProProProProProPro | |
| ENST00000452863.10:c.405_422dup MANE Select | ENSP00000415516.5:p.Pro141_His142insProProProProProPro | |
| ENST00000639563.3:c.405_422dup | ENSP00000492269.3:p.Pro141_His142insProProProProProPro | |
| ENST00000332351.7:c.390_407dup | ENSP00000331327.3:p.Pro136_His137insProProProProProPro | |
| ENST00000379077.7:c.390_407dup | ENSP00000368368.3:p.Pro136_His137insProProProProProPro | |
| ENST00000448076.7:c.390_407dup | ENSP00000413452.3:p.Pro136_His137insProProProProProPro | |
| ENST00000452863.7:c.390_407dup | ENSP00000415516.3:p.Pro136_His137insProProProProProPro | |
| NM_000378.4:c.390_407dup | NP_000369.3:p.Pro136_His137insProProProProProPro | |
| NM_024424.3:c.390_407dup | NP_077742.2:p.Pro136_His137insProProProProProPro | |
| NM_024426.4:c.390_407dup | NP_077744.3:p.Pro136_His137insProProProProProPro | |
| NM_000378.5:c.405_422dup | NP_000369.4:p.Pro141_His142insProProProProProPro | |
| NM_024424.4:c.405_422dup | NP_077742.3:p.Pro141_His142insProProProProProPro | |
| NM_024426.5:c.405_422dup | NP_077744.4:p.Pro141_His142insProProProProProPro | |
| NR_160306.1:n.584_601dup | ||
| NM_000378.6:c.405_422dup | NP_000369.4:p.Pro141_His142insProProProProProPro | |
| NM_024424.5:c.405_422dup | NP_077742.3:p.Pro141_His142insProProProProProPro | |
| NM_024426.6:c.405_422dup MANE Select | NP_077744.4:p.Pro141_His142insProProProProProPro |