Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52029703A>T , CM000666.2:g.52029703A>T | GRCh38 |
| NC_000004.11:g.52895869A>T , CM000666.1:g.52895869A>T | GRCh37 |
| NC_000004.10:g.52590626A>T | NCBI36 |
| NG_008891.1:g.13617T>A , LRG_204:g.13617T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000232.5:c.404T>A MANE Select | NP_000223.1:p.Leu135Ter |
| ENST00000381431.10:c.404T>A MANE Select | ENSP00000370839.6:p.Leu135Ter |
| NM_000232.4:c.404T>A , LRG_204t1:c.404T>A | NP_000223.1:p.Leu135Ter |
| ENST00000381431.9:c.404T>A | ENSP00000370839.5:p.Leu135Ter |
| ENST00000506357.5:c.487T>A | |
| ENST00000514133.1:c.481T>A | ENSP00000425818.1:n.481T>A |
| XM_006714049.2:c.107T>A | XP_006714112.1:p.Leu36Ter |
| XM_011534403.1:c.194T>A | XP_011532705.1:p.Leu65Ter |
| XM_011534404.1:c.107T>A | XP_011532706.1:p.Leu36Ter |