Linked Data
gnomAD v4:
14-91273439-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91273439G>T , CM000676.2:g.91273439G>T | GRCh38 |
| NC_000014.8:g.91739783G>T , CM000676.1:g.91739783G>T | GRCh37 |
| NC_000014.7:g.90809536G>T | NCBI36 |
| NG_033118.1:g.149406C>A | |
| NG_033118.2:g.149406C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5273C>A MANE Select | ENSP00000374507.6:p.Thr1758Asn | |
| ENST00000331194.8:c.845C>A | ENSP00000330332.8:p.Thr282Asn | |
| ENST00000389857.10:c.5273C>A | ENSP00000374507.6:p.Thr1758Asn | |
| ENST00000556726.5:c.1501C>A | ||
| NM_001080414.3:c.5273C>A | NP_001073883.2:p.Thr1758Asn | |
| XM_011536796.1:c.5165C>A | XP_011535098.1:p.Thr1722Asn | |
| XM_011536796.2:c.5165C>A | XP_011535098.1:p.Thr1722Asn | |
| XM_017021336.1:c.2354C>A | XP_016876825.1:p.Thr785Asn | |
| NM_001080414.4:c.5273C>A MANE Select | NP_001073883.2:p.Thr1758Asn |