Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1423789_1423790insGC , CM000667.2:g.1423789_1423790insGC | GRCh38 |
| NC_000005.9:g.1423904_1423905insGC , CM000667.1:g.1423904_1423905insGC | GRCh37 |
| NC_000005.8:g.1476904_1476905insGC | NCBI36 |
| NG_015885.1:g.26639_26640insGC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000270349.12:c.654-1776_654-1775insGC MANE Select | ENSP00000270349.9:n.654-1776_654-1775insG... | |
| ENST00000270349.11:c.654-1776_654-1775insGC | ENSP00000270349.9:n.654-1776_654-1775insG... | |
| NM_001044.4:c.654-1776_654-1775insGC | NP_001035.1:n.654-1776_654-1775insGC | |
| NM_001044.5:c.654-1776_654-1775insGC MANE Select | NP_001035.1:n.654-1776_654-1775insGC |