Linked Data
gnomAD v2:
10-63779851-G-GAAAAA
gnomAD v3:
10-62020092-G-GAAAAA
gnomAD v4:
10-62020092-G-GAAAAA
MyVariant Identifiers:
chr10:g.63779851_63779852insAAAAA (hg19)
chr10:g.62020092_62020093insAAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62020095_62020096insAAAAA , CM000672.2:g.62020095_62020096insAAAAA | GRCh38 |
| NC_000010.10:g.63779854_63779855insAAAAA , CM000672.1:g.63779854_63779855insAAAAA | GRCh37 |
| NC_000010.9:g.63449860_63449861insAAAAA | NCBI36 |
| NG_030027.1:g.123842_123843insAAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279873.12:c.733+19774_733+19775insAAAAA MANE Select | ENSP00000279873.7:n.733+19774_733+19775insAAAAA | |
| ENST00000644638.1:c.734-4578_734-4577insAAAAA | ENSP00000494412.1:n.734-4578_734-4577insAAAAA | |
| ENST00000681100.1:c.733+19774_733+19775insAAAAA | ENSP00000506119.1:n.733+19774_733+19775insAAAAA | |
| ENST00000279873.11:c.733+19774_733+19775insAAAAA | ENSP00000279873.7:n.733+19774_733+19775insAAAAA | |
| NM_032199.2:c.733+19774_733+19775insAAAAA | NP_115575.1:n.733+19774_733+19775insAAAAA | |
| XM_011540262.1:c.503-30793_503-30792insAAAAA | XP_011538564.1:n.503-30793_503-30792insAAAAA | |
| XM_024448230.1:c.166+19774_166+19775insAAAAA | XP_024303998.1:n.166+19774_166+19775insAAAAA | |
| NM_032199.3:c.733+19774_733+19775insAAAAA MANE Select | NP_115575.1:n.733+19774_733+19775insAAAAA |