Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117055_19117060del , CM000669.2:g.19117055_19117060del | GRCh38 |
| NC_000007.13:g.19156678_19156683del , CM000669.1:g.19156678_19156683del | GRCh37 |
| NC_000007.12:g.19123203_19123208del | NCBI36 |
| NG_008114.1:g.5622_5627del | |
| NG_008114.2:g.5622_5627del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.271_276del MANE Select | ENSP00000242261.5:p.Gly91_Gly92del | |
| ENST00000242261.5:c.271_276del | ENSP00000242261.5:p.Gly91_Gly92del | |
| ENST00000354571.5:c.68_73del | ||
| NM_000474.3:c.271_276del | NP_000465.1:p.Gly91_Gly92del | |
| XM_011515496.1:c.271_276del | XP_011513798.1:p.Gly91_Gly92del | |
| NR_149001.1:n.622_627del | ||
| NM_000474.4:c.271_276del MANE Select | NP_000465.1:p.Gly91_Gly92del | |
| NR_149001.2:n.586_591del |