Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.44540940_44540941insAT , CM000685.2:g.44540940_44540941insAT | GRCh38 |
| NC_000023.10:g.44400186_44400187insAT , CM000685.1:g.44400186_44400187insAT | GRCh37 |
| NC_000023.9:g.44285130_44285131insAT | NCBI36 |
| NG_021288.1:g.7035_7036insAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378045.5:c.185+1004_185+1005insAT MANE Select | ENSP00000367284.4:n.185+1004_185+1005insAT | |
| ENST00000378045.4:c.185+1004_185+1005insAT | ENSP00000367284.4:n.185+1004_185+1005insAT | |
| ENST00000483115.1:n.360+1004_360+1005insAT | ||
| NM_173794.3:c.185+1004_185+1005insAT | NP_776155.1:n.185+1004_185+1005insAT | |
| NM_173794.4:c.185+1004_185+1005insAT MANE Select | NP_776155.1:n.185+1004_185+1005insAT |