Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1395129_1395132delinsCGTG , CM000667.2:g.1395129_1395132delinsCGTG | GRCh38 |
| NC_000005.9:g.1395244_1395247delinsCGTG , CM000667.1:g.1395244_1395247delinsCGTG | GRCh37 |
| NC_000005.8:g.1448244_1448247delinsCGTG | NCBI36 |
| NG_015885.1:g.55297_55300delinsCACG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1840-374_1840-371delinsCACG MANE Select | ENSP00000270349.9:n.1840-374_1840-371delinsCACG | |
| ENST00000270349.11:c.1840-374_1840-371delinsCACG | ENSP00000270349.9:n.1840-374_1840-371delinsCACG | |
| ENST00000512002.2:n.221-374_221-371delinsCACG | ||
| NM_001044.4:c.1840-374_1840-371delinsCACG | NP_001035.1:n.1840-374_1840-371delinsCACG | |
| NM_001044.5:c.1840-374_1840-371delinsCACG MANE Select | NP_001035.1:n.1840-374_1840-371delinsCACG |