Linked Data
dbSNP Id:
rs894281957
MyVariant Identifiers:
chr16:g.17231973_17231974insTAAT (hg19)
chr16:g.17138116_17138117insTAAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17138117_17138120dup , CM000678.2:g.17138117_17138120dup | GRCh38 |
| NC_000016.9:g.17231974_17231977dup , CM000678.1:g.17231974_17231977dup | GRCh37 |
| NC_000016.8:g.17139475_17139478dup | NCBI36 |
| NG_015843.1:g.337762_337765dup | |
| NG_015843.2:g.337762_337765dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261381.7:c.1764+235_1764+238dup MANE Select | ENSP00000261381.6:n.1764+235_1764+238dup | |
| ENST00000261381.6:c.1764+235_1764+238dup | ENSP00000261381.6:n.1764+235_1764+238dup | |
| NM_022166.3:c.1764+235_1764+238dup | NP_071449.1:n.1764+235_1764+238dup | |
| XM_011522574.1:c.1764+235_1764+238dup | XP_011520876.1:n.1764+235_1764+238dup | |
| XR_933140.1:n.336-125_336-122dup | ||
| XR_933141.1:n.175-125_175-122dup | ||
| XR_933143.1:n.237-125_237-122dup | ||
| NR_135179.1:n.147-125_147-122dup | ||
| XM_017023539.2:c.1764+235_1764+238dup | XP_016879028.1:n.1764+235_1764+238dup | |
| XM_017023540.2:c.1764+235_1764+238dup | XP_016879029.1:n.1764+235_1764+238dup | |
| NM_022166.4:c.1764+235_1764+238dup MANE Select | NP_071449.1:n.1764+235_1764+238dup |