Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14139268A>T , CM000665.2:g.14139268A>T | GRCh38 |
| NC_000003.11:g.14180768A>T , CM000665.1:g.14180768A>T | GRCh37 |
| NC_000003.10:g.14155769A>T | NCBI36 |
| NG_008975.1:g.19329A>T , LRG_435:g.19329A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*1001A>T | ENSP00000395617.1:n.*1001A>T | |
| ENST00000306077.5:c.971A>T MANE Select | ENSP00000303992.5:p.Asn324Ile | |
| ENST00000306077.4:c.971A>T | ENSP00000303992.4:p.Asn324Ile | |
| ENST00000601399.3:n.298A>T | ||
| ENST00000608606.1:c.207A>T | ||
| NM_024334.2:c.971A>T , LRG_435t1:c.971A>T | NP_077310.1:p.Asn324Ile | |
| XM_011534109.1:c.866A>T | XP_011532411.1:p.Asn289Ile | |
| XM_017007176.2:c.866A>T | XP_016862665.1:p.Asn289Ile | |
| NM_024334.3:c.971A>T MANE Select | NP_077310.1:p.Asn324Ile |