Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8015298_8015299delinsGA , CM000679.2:g.8015298_8015299delinsGA | GRCh38 |
| NC_000017.10:g.7918616_7918617delinsGA , CM000679.1:g.7918616_7918617delinsGA | GRCh37 |
| NC_000017.9:g.7859341_7859342delinsGA | NCBI36 |
| NG_009092.1:g.17629_17630delinsGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.2770-30_2770-29delinsGA MANE Select | ENSP00000254854.4:n.2770-30_2770-29delinsGA | |
| ENST00000254854.4:c.2770-30_2770-29delinsGA | ENSP00000254854.4:n.2770-30_2770-29delinsGA | |
| NM_000180.3:c.2770-30_2770-29delinsGA | NP_000171.1:n.2770-30_2770-29delinsGA | |
| XM_011523816.1:c.2770-30_2770-29delinsGA | XP_011522118.1:n.2770-30_2770-29delinsGA | |
| NM_000180.4:c.2770-30_2770-29delinsGA MANE Select | NP_000171.1:n.2770-30_2770-29delinsGA |