Linked Data
ClinVar Variation Id:
375524
ClinVar RCV Id:
RCV000417015
dbSNP Id:
rs1057519542
MyVariant Identifiers:
chrX:g.18622493_18622496dupGACC (hg19)
chrX:g.18604373_18604376dupGACC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18604373_18604376dup , CM000685.2:g.18604373_18604376dup | GRCh38 |
| NC_000023.10:g.18622493_18622496dup , CM000685.1:g.18622493_18622496dup | GRCh37 |
| NC_000023.9:g.18532414_18532417dup | NCBI36 |
| NG_008475.1:g.183769_183772dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000623535.2:c.1449_1452dup MANE Select | ENSP00000485244.1:p.Lys485AspfsTer11 | |
| ENST00000635828.1:c.1449_1452dup | ENSP00000490170.1:p.Lys485AspfsTer11 | |
| ENST00000674046.1:c.1449_1452dup | ENSP00000501174.1:p.Lys485AspfsTer11 | |
| ENST00000379989.6:c.1449_1452dup | ENSP00000369325.3:p.Lys485AspfsTer11 | |
| ENST00000379996.7:c.1449_1452dup | ENSP00000369332.3:p.Lys485AspfsTer11 | |
| ENST00000463994.4:c.1449_1452dup | ENSP00000485184.1:p.Lys485AspfsTer11 | |
| ENST00000623535.1:c.1449_1452dup | ENSP00000485244.1:p.Lys485AspfsTer11 | |
| NM_001037343.1:c.1449_1452dup | NP_001032420.1:p.Lys485AspfsTer11 | |
| NM_003159.2:c.1449_1452dup | NP_003150.1:p.Lys485AspfsTer11 | |
| XM_011545569.1:c.1398_1401dup | XP_011543871.1:p.Lys468AspfsTer11 | |
| XM_011545570.1:c.1317_1320dup | XP_011543872.1:p.Lys441AspfsTer11 | |
| XR_950484.1:n.1701_1704dup | ||
| NM_001323289.1:c.1449_1452dup | NP_001310218.1:p.Lys485AspfsTer11 | |
| NM_001323289.2:c.1449_1452dup MANE Select | NP_001310218.1:p.Lys485AspfsTer11 | |
| NM_001037343.2:c.1449_1452dup | NP_001032420.1:p.Lys485AspfsTer11 | |
| NM_003159.3:c.1449_1452dup | NP_003150.1:p.Lys485AspfsTer11 |