Linked Data
dbSNP Id:
rs1165672838
gnomAD v2:
16-17232436-C-CAGATGAACT
gnomAD v4:
16-17138579-C-CAGATGAACT
MyVariant Identifiers:
chr16:g.17232436_17232437insAGATGAACT (hg19)
chr16:g.17138579_17138580insAGATGAACT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17138580_17138588dup , CM000678.2:g.17138580_17138588dup | GRCh38 |
| NC_000016.9:g.17232437_17232445dup , CM000678.1:g.17232437_17232445dup | GRCh37 |
| NC_000016.8:g.17139938_17139946dup | NCBI36 |
| NG_015843.1:g.337294_337302dup | |
| NG_015843.2:g.337294_337302dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261381.7:c.1588-57_1588-49dup MANE Select | ENSP00000261381.6:n.1588-57_1588-49dup | |
| ENST00000261381.6:c.1588-57_1588-49dup | ENSP00000261381.6:n.1588-57_1588-49dup | |
| NM_022166.3:c.1588-57_1588-49dup | NP_071449.1:n.1588-57_1588-49dup | |
| XM_011522574.1:c.1588-57_1588-49dup | XP_011520876.1:n.1588-57_1588-49dup | |
| XR_933141.1:n.513_521dup | ||
| NR_135179.1:n.485_493dup | ||
| XM_017023539.2:c.1588-57_1588-49dup | XP_016879028.1:n.1588-57_1588-49dup | |
| XM_017023540.2:c.1588-57_1588-49dup | XP_016879029.1:n.1588-57_1588-49dup | |
| NM_022166.4:c.1588-57_1588-49dup MANE Select | NP_071449.1:n.1588-57_1588-49dup |