Linked Data
dbSNP Id:
rs1555454543
gnomAD v2:
15-72103795-T-TGCCCC
gnomAD v3:
15-71811455-T-TGCCCC
gnomAD v4:
15-71811455-T-TGCCCC
MyVariant Identifiers:
chr15:g.72103795_72103796insGCCCC (hg19)
chr15:g.71811455_71811456insGCCCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.71811456_71811457insCCCCG , CM000677.2:g.71811456_71811457insCCCCG | GRCh38 |
| NC_000015.9:g.72103796_72103797insCCCCG , CM000677.1:g.72103796_72103797insCCCCG | GRCh37 |
| NC_000015.8:g.69890850_69890851insCCCCG | NCBI36 |
| NG_009113.2:g.5902_5903insCCCCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617575.5:c.119-27_119-26insCCCCG MANE Select | ENSP00000482504.1:n.119-27_119-26insCCCCG | |
| ENST00000617575.4:c.119-27_119-26insCCCCG | ENSP00000482504.1:n.119-27_119-26insCCCCG | |
| ENST00000621098.1:c.119-27_119-26insCCCCG | ENSP00000479962.1:n.119-27_119-26insCCCCG | |
| ENST00000621736.4:c.-146-27_-146-26insCCCCG | ENSP00000479254.1:n.-146-27_-146-26insCCCCG | |
| NM_014249.3:c.119-27_119-26insCCCCG | NP_055064.1:n.119-27_119-26insCCCCG | |
| NM_016346.3:c.119-27_119-26insCCCCG | NP_057430.1:n.119-27_119-26insCCCCG | |
| XM_011521146.1:c.-146-27_-146-26insCCCCG | XP_011519448.1:n.-146-27_-146-26insCCCCG | |
| NM_014249.4:c.119-27_119-26insCCCCG MANE Select | NP_055064.1:n.119-27_119-26insCCCCG | |
| NM_016346.4:c.119-27_119-26insCCCCG | NP_057430.1:n.119-27_119-26insCCCCG |