Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8012366_8012367insACA , CM000679.2:g.8012366_8012367insACA | GRCh38 |
| NC_000017.10:g.7915684_7915685insACA , CM000679.1:g.7915684_7915685insACA | GRCh37 |
| NC_000017.9:g.7856409_7856410insACA | NCBI36 |
| NG_009092.1:g.14697_14698insACA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.1956+16_1956+17insACA MANE Select | ENSP00000254854.4:n.1956+16_1956+17insACA | |
| ENST00000254854.4:c.1956+16_1956+17insACA | ENSP00000254854.4:n.1956+16_1956+17insACA | |
| NM_000180.3:c.1956+16_1956+17insACA | NP_000171.1:n.1956+16_1956+17insACA | |
| XM_011523816.1:c.1956+16_1956+17insACA | XP_011522118.1:n.1956+16_1956+17insACA | |
| NM_000180.4:c.1956+16_1956+17insACA MANE Select | NP_000171.1:n.1956+16_1956+17insACA |