Linked Data
ClinVar Variation Id:
1958568
ClinVar RCV Id:
RCV002725525
gnomAD v4:
22-50526358-C-T
MyVariant Identifiers:
chr22:g.50964787C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50526358C>T , CM000684.2:g.50526358C>T | GRCh38 |
| NC_000022.10:g.50964787C>T , CM000684.1:g.50964787C>T | GRCh37 |
| NC_000022.9:g.49311653C>T | NCBI36 |
| NG_011860.1:g.8728G>A , LRG_727:g.8728G>A | |
| NG_016235.1:g.5082G>A | |
| NG_021419.1:g.23143C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252029.8:c.1047G>A (TYMP) MANE Select | ENSP00000252029.3:p.Ala349= | |
| ENST00000395680.6:c.1047G>A (TYMP) | ENSP00000379037.1:p.Ala349= | |
| ENST00000395681.6:c.1047G>A (TYMP) | ENSP00000379038.1:p.Ala349= | |
| ENST00000543927.6:c.-126G>A (SCO2) | ENSP00000444433.1:n.-126G>A | |
| ENST00000650719.1:c.928G>A (TYMP) | ENSP00000498276.1:p.Ala310Thr | |
| ENST00000652401.1:c.548G>A (TYMP) | ||
| ENST00000252029.7:c.1047G>A (TYMP) | ENSP00000252029.3:p.Ala349= | |
| ENST00000395678.7:c.1047G>A (TYMP) | ENSP00000379036.3:p.Ala349= | |
| ENST00000395680.5:c.1047G>A (TYMP) | ENSP00000379037.1:p.Ala349= | |
| ENST00000395681.5:c.1047G>A (TYMP) | ENSP00000379038.1:p.Ala349= | |
| ENST00000423348.1:c.-126G>A | ENSP00000403570.1:n.-126G>A | |
| ENST00000425169.1:c.948G>A (TYMP) | ENSP00000395875.1:p.Ala316= | |
| ENST00000476284.1:n.1053G>A (TYMP) | ||
| ENST00000487577.5:n.1334G>A (TYMP) | ||
| ENST00000543927.5:c.-126G>A | ENSP00000444433.1:n.-126G>A | |
| NM_001113755.2:c.1047G>A (TYMP) | NP_001107227.1:p.Ala349= | |
| NM_001113756.2:c.1047G>A (TYMP) | NP_001107228.1:p.Ala349= | |
| NM_001169109.1:c.-126G>A (SCO2) | NP_001162580.1:n.-126G>A | |
| NM_001257988.1:c.1047G>A , LRG_727t1:c.1047G>A (TYMP) | NP_001244917.1:p.Ala349= | |
| NM_001257989.1:c.1047G>A , LRG_727t2:c.1047G>A (TYMP) | NP_001244918.1:p.Ala349= | |
| NM_001953.4:c.1047G>A (TYMP) | NP_001944.1:p.Ala349= | |
| NM_001113755.3:c.1047G>A (TYMP) | NP_001107227.1:p.Ala349= | |
| NM_001113756.3:c.1047G>A (TYMP) | NP_001107228.1:p.Ala349= | |
| NM_001953.5:c.1047G>A (TYMP) MANE Select | NP_001944.1:p.Ala349= | |
| NM_001169109.2:c.-126G>A (SCO2) | NP_001162580.1:n.-126G>A |