Linked Data
dbSNP Id:
rs1566275140
gnomAD v2:
13-25457390-TTGA-T
gnomAD v4:
13-24883252-TTGA-T
MyVariant Identifiers:
chr13:g.25457391_25457393del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.24883256_24883258del , CM000675.2:g.24883256_24883258del | GRCh38 |
| NC_000013.10:g.25457394_25457396del , CM000675.1:g.25457394_25457396del | GRCh37 |
| NC_000013.9:g.24355394_24355396del | NCBI36 |
| NG_009165.2:g.44693_44695del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381884.9:c.3939_3941del (CENPJ) MANE Select | ENSP00000371308.4:p.His1313del | |
| ENST00000545981.6:c.*679_*681del (CENPJ) | ENSP00000441090.2:n.*679_*681del | |
| ENST00000381884.8:c.3939_3941del (CENPJ) | ENSP00000371308.4:p.His1313del | |
| ENST00000545981.5:c.*680_*682del (CENPJ) | ENSP00000441090.2:n.*680_*682del | |
| ENST00000616936.4:c.*593_*595del (CENPJ) | ENSP00000477511.1:n.*593_*595del | |
| NM_018451.4:c.3939_3941del (CENPJ) | NP_060921.3:p.His1313del | |
| NR_047594.1:n.4251_4253del (CENPJ) | ||
| NR_047595.1:n.4049_4051del (CENPJ) | ||
| XM_011535156.1:c.*10+3961_*10+3963del (RNF17) | XP_011533458.1:n.*10+3961_*10+3963del | |
| XM_011535156.2:c.*10+3961_*10+3963del (RNF17) | XP_011533458.1:n.*10+3961_*10+3963del | |
| NM_018451.5:c.3939_3941del (CENPJ) MANE Select | NP_060921.3:p.His1313del | |
| NR_047594.2:n.4223_4225del (CENPJ) | ||
| NR_047595.2:n.4021_4023del (CENPJ) |