Linked Data
gnomAD v2:
10-64291378-C-CAAAA
gnomAD v3:
10-62531619-C-CAAAA
gnomAD v4:
10-62531619-C-CAAAA
MyVariant Identifiers:
chr10:g.64291378_64291379insAAAA (hg19)
chr10:g.62531619_62531620insAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.62531619_62531620insAAAA , CM000672.2:g.62531619_62531620insAAAA | GRCh38 |
| NC_000010.10:g.64291378_64291379insAAAA , CM000672.1:g.64291378_64291379insAAAA | GRCh37 |
| NC_000010.9:g.63961384_63961385insAAAA | NCBI36 |
| NG_021209.1:g.162463_162464insAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647733.1:c.981+71822_981+71823insAAAA | ENSP00000502188.1:n.981+71822_981+71823insAAAA | |
| ENST00000395251.5:c.-185+11022_-185+11023insAAAA | ENSP00000378672.1:n.-185+11022_-185+11023insAAAA | |
| ENST00000410046.7:c.981+71822_981+71823insAAAA | ENSP00000387091.3:n.981+71822_981+71823insAAAA | |
| NM_199451.2:c.981+71822_981+71823insAAAA | NP_955523.1:n.981+71822_981+71823insAAAA | |
| NM_199452.3:c.-185+11022_-185+11023insAAAA | NP_955524.3:n.-185+11022_-185+11023insAAAA | |
| XM_017015937.2:c.982-12590_982-12589insAAAA | XP_016871426.1:n.982-12590_982-12589insAAAA | |
| NM_199451.3:c.981+71822_981+71823insAAAA | NP_955523.1:n.981+71822_981+71823insAAAA |