Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965588dup , CM000670.2:g.37965588dup | GRCh38 |
| NC_000008.10:g.37823106dup , CM000670.1:g.37823106dup | GRCh37 |
| NC_000008.9:g.37942263dup | NCBI36 |
| NG_011936.1:g.6081dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.884dup MANE Select | ENSP00000343782.3:p.Leu296SerfsTer? | |
| ENST00000520341.2:n.1012dup | ||
| ENST00000647937.1:c.368dup | ENSP00000497740.1:p.Leu124SerfsTer? | |
| ENST00000345060.4:c.884dup | ENSP00000343782.3:p.Leu296SerfsTer? | |
| ENST00000520341.1:n.159dup | ||
| ENST00000614635.1:c.884dup | ENSP00000480325.1:p.Leu296SerfsTer? | |
| NM_000025.2:c.884dup | NP_000016.1:p.Leu296SerfsTer? | |
| NM_000025.3:c.884dup MANE Select | NP_000016.1:p.Leu296SerfsTer? |