Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.87616358_87616361del , CM000666.2:g.87616358_87616361del | GRCh38 |
| NC_000004.11:g.88537510_88537513del , CM000666.1:g.88537510_88537513del | GRCh37 |
| NC_000004.10:g.88756534_88756537del | NCBI36 |
| NG_011595.1:g.12830_12833del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014208.3:c.3696_3699del MANE Select | NP_055023.2:p.Asn1232LysfsTer? |
| ENST00000651931.1:c.3696_3699del MANE Select | ENSP00000498766.1:p.Asn1232LysfsTer? |
| ENST00000282478.7:c.3696_3699del | ENSP00000282478.7:p.Asn1232LysfsTer? |
| ENST00000399271.5:c.3696_3699del | ENSP00000382213.1:p.Asn1232LysfsTer? |