Linked Data
dbSNP Id:
rs1555422043
gnomAD v3:
15-42401485-C-CCCCT
gnomAD v4:
15-42401485-C-CCCCT
MyVariant Identifiers:
chr15:g.42693683_42693684insCCCT (hg19)
chr15:g.42401485_42401486insCCCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42401487_42401488insCTCC , CM000677.2:g.42401487_42401488insCTCC | GRCh38 |
| NC_000015.9:g.42693685_42693686insCTCC , CM000677.1:g.42693685_42693686insCTCC | GRCh37 |
| NC_000015.8:g.40480977_40480978insCTCC | NCBI36 |
| NG_008660.1:g.58385_58386insCTCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1211-154_1211-153insCTCC | ENSP00000183936.4:n.1211-154_1211-153insCTCC | |
| ENST00000357568.8:c.1355-154_1355-153insCTCC | ENSP00000350181.3:n.1355-154_1355-153insCTCC | |
| ENST00000397163.8:c.1355-154_1355-153insCTCC MANE Select | ENSP00000380349.3:n.1355-154_1355-153insCTCC | |
| ENST00000466369.5:n.1864-154_1864-153insCTCC | ||
| ENST00000483208.5:n.1586-154_1586-153insCTCC | ||
| ENST00000495723.1:n.1586-154_1586-153insCTCC | ||
| ENST00000549793.5:n.1586-154_1586-153insCTCC | ||
| ENST00000638141.2:n.1226-154_1226-153insCTCC | ||
| ENST00000673705.1:c.309+1835_309+1836insCTCC | ENSP00000501021.1:n.309+1835_309+1836insCTCC | |
| ENST00000318023.11:c.1211-154_1211-153insCTCC | ENSP00000326281.8:n.1211-154_1211-153insCTCC | |
| ENST00000349748.7:c.1211-154_1211-153insCTCC | ENSP00000183936.4:n.1211-154_1211-153insCTCC | |
| ENST00000357568.7:c.1355-154_1355-153insCTCC | ENSP00000350181.3:n.1355-154_1355-153insCTCC | |
| ENST00000397163.7:c.1355-154_1355-153insCTCC | ENSP00000380349.3:n.1355-154_1355-153insCTCC | |
| NM_000070.2:c.1355-154_1355-153insCTCC | NP_000061.1:n.1355-154_1355-153insCTCC | |
| NM_024344.1:c.1355-154_1355-153insCTCC | NP_077320.1:n.1355-154_1355-153insCTCC | |
| NM_173087.1:c.1211-154_1211-153insCTCC | NP_775110.1:n.1211-154_1211-153insCTCC | |
| NM_000070.3:c.1355-154_1355-153insCTCC MANE Select | NP_000061.1:n.1355-154_1355-153insCTCC | |
| NM_024344.2:c.1355-154_1355-153insCTCC | NP_077320.1:n.1355-154_1355-153insCTCC | |
| NM_173087.2:c.1211-154_1211-153insCTCC | NP_775110.1:n.1211-154_1211-153insCTCC |