Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.61531938_61531942del , CM000682.2:g.61531938_61531942del | GRCh38 |
| NC_000020.10:g.60106994_60106998del , CM000682.1:g.60106994_60106998del | GRCh37 |
| NC_000020.9:g.59540389_59540393del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614565.5:c.170-211625_170-211621del MANE Select | ENSP00000484928.1:n.170-211625_170-211621del | |
| ENST00000614565.4:c.170-211625_170-211621del | ENSP00000484928.1:n.170-211625_170-211621del | |
| NM_001252338.2:c.58+32446_58+32450del | NP_001239267.1:n.58+32446_58+32450del | |
| NM_001794.4:c.170-211625_170-211621del | NP_001785.2:n.170-211625_170-211621del | |
| NM_001794.5:c.170-211625_170-211621del MANE Select | NP_001785.2:n.170-211625_170-211621del |