Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49459216_49459228del , CM000668.2:g.49459216_49459228del | GRCh38 |
| NC_000006.11:g.49426929_49426941del , CM000668.1:g.49426929_49426941del | GRCh37 |
| NC_000006.10:g.49534888_49534900del | NCBI36 |
| NG_007100.1:g.8916_8928del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.243_255del MANE Select | ENSP00000274813.3:p.Leu81PhefsTer4 | |
| ENST00000274813.3:c.243_255del | ENSP00000274813.3:p.Leu81PhefsTer4 | |
| NM_000255.3:c.243_255del | NP_000246.2:p.Leu81PhefsTer4 | |
| XM_005249143.2:c.243_255del | XP_005249200.1:p.Leu81PhefsTer4 | |
| XM_005249143.3:c.243_255del | XP_005249200.1:p.Leu81PhefsTer4 | |
| NM_000255.4:c.243_255del MANE Select | NP_000246.2:p.Leu81PhefsTer4 |