Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48342631G>A , CM000675.2:g.48342631G>A | GRCh38 |
| NC_000013.10:g.48916767G>A , CM000675.1:g.48916767G>A | GRCh37 |
| NC_000013.9:g.47814768G>A | NCBI36 |
| NG_009009.1:g.43885G>A , LRG_517:g.43885G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.297G>A MANE Select | ENSP00000267163.4:p.Trp99Ter | |
| ENST00000650461.1:c.297G>A | ENSP00000497193.1:p.Trp99Ter | |
| ENST00000267163.4:c.297G>A | ENSP00000267163.4:p.Trp99Ter | |
| ENST00000467505.5:c.138-17386G>A | ENSP00000434702.1:n.138-17386G>A | |
| ENST00000525036.1:n.459G>A | ||
| NM_000321.2:c.297G>A , LRG_517t1:c.297G>A | NP_000312.2:p.Trp99Ter | |
| XM_011535171.1:c.36G>A | XP_011533473.1:p.Trp12Ter | |
| XM_011535171.2:c.36G>A | XP_011533473.1:p.Trp12Ter | |
| NM_000321.3:c.297G>A MANE Select | NP_000312.2:p.Trp99Ter |