Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91273395G>A , CM000676.2:g.91273395G>A | GRCh38 |
| NC_000014.8:g.91739739G>A , CM000676.1:g.91739739G>A | GRCh37 |
| NC_000014.7:g.90809492G>A | NCBI36 |
| NG_033118.1:g.149450C>T | |
| NG_033118.2:g.149450C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5317C>T MANE Select | ENSP00000374507.6:p.Pro1773Ser | |
| ENST00000331194.8:c.889C>T | ENSP00000330332.8:p.Pro297Ser | |
| ENST00000389857.10:c.5317C>T | ENSP00000374507.6:p.Pro1773Ser | |
| ENST00000556726.5:c.1545C>T | ||
| NM_001080414.3:c.5317C>T | NP_001073883.2:p.Pro1773Ser | |
| XM_011536796.1:c.5209C>T | XP_011535098.1:p.Pro1737Ser | |
| XM_011536796.2:c.5209C>T | XP_011535098.1:p.Pro1737Ser | |
| XM_017021336.1:c.2398C>T | XP_016876825.1:p.Pro800Ser | |
| NM_001080414.4:c.5317C>T MANE Select | NP_001073883.2:p.Pro1773Ser |