Linked Data
dbSNP Id:
rs1398447966
gnomAD v3:
15-42401473-G-GCGC
gnomAD v4:
15-42401473-G-GCGC
MyVariant Identifiers:
chr15:g.42693671_42693672insCGC (hg19)
chr15:g.42401473_42401474insCGC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42401474_42401475insGCC , CM000677.2:g.42401474_42401475insGCC | GRCh38 |
| NC_000015.9:g.42693672_42693673insGCC , CM000677.1:g.42693672_42693673insGCC | GRCh37 |
| NC_000015.8:g.40480964_40480965insGCC | NCBI36 |
| NG_008660.1:g.58372_58373insGCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1211-167_1211-166insGCC | ENSP00000183936.4:n.1211-167_1211-166insGCC | |
| ENST00000357568.8:c.1355-167_1355-166insGCC | ENSP00000350181.3:n.1355-167_1355-166insGCC | |
| ENST00000397163.8:c.1355-167_1355-166insGCC MANE Select | ENSP00000380349.3:n.1355-167_1355-166insGCC | |
| ENST00000466369.5:n.1864-167_1864-166insGCC | ||
| ENST00000483208.5:n.1586-167_1586-166insGCC | ||
| ENST00000495723.1:n.1586-167_1586-166insGCC | ||
| ENST00000549793.5:n.1586-167_1586-166insGCC | ||
| ENST00000638141.2:n.1226-167_1226-166insGCC | ||
| ENST00000673705.1:c.309+1822_309+1823insGCC | ENSP00000501021.1:n.309+1822_309+1823insGCC | |
| ENST00000318023.11:c.1211-167_1211-166insGCC | ENSP00000326281.8:n.1211-167_1211-166insGCC | |
| ENST00000349748.7:c.1211-167_1211-166insGCC | ENSP00000183936.4:n.1211-167_1211-166insGCC | |
| ENST00000357568.7:c.1355-167_1355-166insGCC | ENSP00000350181.3:n.1355-167_1355-166insGCC | |
| ENST00000397163.7:c.1355-167_1355-166insGCC | ENSP00000380349.3:n.1355-167_1355-166insGCC | |
| NM_000070.2:c.1355-167_1355-166insGCC | NP_000061.1:n.1355-167_1355-166insGCC | |
| NM_024344.1:c.1355-167_1355-166insGCC | NP_077320.1:n.1355-167_1355-166insGCC | |
| NM_173087.1:c.1211-167_1211-166insGCC | NP_775110.1:n.1211-167_1211-166insGCC | |
| NM_000070.3:c.1355-167_1355-166insGCC MANE Select | NP_000061.1:n.1355-167_1355-166insGCC | |
| NM_024344.2:c.1355-167_1355-166insGCC | NP_077320.1:n.1355-167_1355-166insGCC | |
| NM_173087.2:c.1211-167_1211-166insGCC | NP_775110.1:n.1211-167_1211-166insGCC |