Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21854340G>A , CM000669.2:g.21854340G>A | GRCh38 |
| NC_000007.13:g.21893958G>A , CM000669.1:g.21893958G>A | GRCh37 |
| NC_000007.12:g.21860483G>A | NCBI36 |
| NG_012886.2:g.316126G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.11087G>A MANE Select | NP_001264044.1:p.Arg3696Lys |
| ENST00000409508.8:c.11087G>A MANE Select | ENSP00000475939.1:p.Arg3696Lys |
| NM_001277115.1:c.11087G>A | NP_001264044.1:p.Arg3696Lys |
| ENST00000328843.10:c.11108G>A | ENSP00000330671.7:p.Arg3703Lys |
| ENST00000409508.7:c.11087G>A | ENSP00000475939.1:p.Arg3696Lys |
| ENST00000421290.1:n.270G>A | |
| ENST00000607413.5:n.350G>A | |
| ENST00000620169.4:c.11108G>A | ENSP00000481693.1:p.Arg3703Lys |