Linked Data
dbSNP Id:
rs1333637219
gnomAD v3:
15-22825304-T-TA
gnomAD v4:
15-22825304-T-TA
MyVariant Identifiers:
chr15:g.22825304_22825305insA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22825305dup , CM000677.2:g.22825305dup | GRCh38 |
| NC_000015.9:g.23047763dup , CM000677.1:g.23047763dup | GRCh37 |
| NC_000015.8:g.20599204dup | NCBI36 |
| NG_009056.1:g.44081dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337435.9:c.*1066dup MANE Select | ENSP00000337452.4:n.*1066dup | |
| ENST00000337435.8:c.*1066dup | ENSP00000337452.4:n.*1066dup | |
| ENST00000437912.6:c.*1066dup | ENSP00000393962.2:n.*1066dup | |
| ENST00000559448.5:c.2028dup | ||
| NM_001142275.1:c.*1066dup | NP_001135747.1:n.*1066dup | |
| NM_144599.4:c.*1066dup | NP_653200.2:n.*1066dup | |
| NM_144599.5:c.*1066dup MANE Select | NP_653200.2:n.*1066dup |