Linked Data
dbSNP Id:
rs781530400
gnomAD v2:
14-91772265-T-TGCATTCTA
gnomAD v3:
14-91305921-T-TGCATTCTA
gnomAD v4:
14-91305921-T-TGCATTCTA
MyVariant Identifiers:
chr14:g.91772265_91772266insGCATTCTA (hg19)
chr14:g.91305921_91305922insGCATTCTA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91305923_91305930dup , CM000676.2:g.91305923_91305930dup | GRCh38 |
| NC_000014.8:g.91772267_91772274dup , CM000676.1:g.91772267_91772274dup | GRCh37 |
| NC_000014.7:g.90842020_90842027dup | NCBI36 |
| NG_033118.1:g.116916_116923dup | |
| NG_033118.2:g.116916_116923dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.3196-3_3200dup | ||
| ENST00000389857.10:c.3196-3_3200dup | ||
| NM_001080414.3:c.3196-3_3200dup | ||
| XM_005267691.3:c.3196-3_3200dup | ||
| XM_011536796.1:c.3088-3_3092dup | ||
| XR_429316.2:n.3324-3_3328dup | ||
| XR_943459.1:n.3324-3_3328dup | ||
| XM_005267691.5:c.3196-3_3200dup | ||
| XM_011536796.2:c.3088-3_3092dup | ||
| XM_017021335.2:c.3196-3_3200dup | ||
| XM_017021336.1:c.277-3_281dup | ||
| XR_429316.4:n.3322-3_3326dup | ||
| NM_001080414.4:c.3196-3_3200dup |