Linked Data
MyVariant Identifiers:
chr1:g.55518679_55518680insG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55053007dup , CM000663.2:g.55053007dup | GRCh38 |
| NC_000001.10:g.55518680dup , CM000663.1:g.55518680dup | GRCh37 |
| NC_000001.9:g.55291268dup | NCBI36 |
| NG_009061.1:g.18461dup , LRG_275:g.18461dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.799+216dup | ENSP00000501161.2:n.799+216dup | |
| ENST00000710286.1:c.1156+216dup | ENSP00000518176.1:n.1156+216dup | |
| ENST00000673903.1:c.424+216dup | ENSP00000501257.1:n.424+216dup | |
| ENST00000302118.5:c.799+216dup MANE Select | ENSP00000303208.5:n.799+216dup | |
| ENST00000490692.1:n.1620+216dup | ||
| NM_174936.3:c.799+216dup , LRG_275t1:c.799+216dup | NP_777596.2:n.799+216dup | |
| NR_110451.1:n.458+216dup | ||
| NM_174936.4:c.799+216dup MANE Select | NP_777596.2:n.799+216dup | |
| NR_110451.2:n.458+216dup |