Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47342680G>A , CM000673.2:g.47342680G>A | GRCh38 |
| NC_000011.9:g.47364231G>A , CM000673.1:g.47364231G>A | GRCh37 |
| NC_000011.8:g.47320807G>A | NCBI36 |
| NG_007667.1:g.15023C>T , LRG_386:g.15023C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.1522C>T MANE Select | ENSP00000442795.1:p.Gln508Ter | |
| ENST00000256993.8:c.1522C>T | ENSP00000256993.5:p.Gln508Ter | |
| ENST00000399249.6:c.1522C>T | ENSP00000382193.2:p.Gln508Ter | |
| ENST00000544791.1:c.1522C>T | ENSP00000444259.1:p.Gln508Ter | |
| ENST00000545968.5:c.1522C>T | ENSP00000442795.1:p.Gln508Ter | |
| NM_000256.3:c.1522C>T , LRG_386t1:c.1522C>T MANE Select | NP_000247.2:p.Gln508Ter | |
| XM_011520117.1:c.1504C>T | XP_011518419.1:p.Gln502Ter | |
| XM_011520118.1:c.1522C>T | XP_011518420.1:p.Gln508Ter |