UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28484009G>T , CM000678.2:g.28484009G>T | GRCh38 |
| NC_000016.9:g.28495330G>T , CM000678.1:g.28495330G>T | GRCh37 |
| NC_000016.8:g.28402831G>T | NCBI36 |
| NG_008654.2:g.13294C>A , LRG_689:g.13294C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333496.14:c.715C>A | ENSP00000329171.9:p.Pro239Thr | |
| ENST00000355477.10:c.643C>A | ENSP00000347660.7:p.Pro215Thr | |
| ENST00000357857.14:c.625C>A | ENSP00000350523.9:p.Pro209Thr | |
| ENST00000359984.12:c.787C>A | ENSP00000353073.9:p.Pro263Thr | |
| ENST00000360019.8:c.715C>A | ENSP00000353116.3:p.Pro239Thr | |
| ENST00000395653.9:c.328C>A | ENSP00000379014.5:p.Pro110Thr | |
| ENST00000561689.6:n.1072C>A | ||
| ENST00000564091.6:c.127C>A | ENSP00000454466.2:p.Pro43Thr | |
| ENST00000565316.6:c.787C>A | ENSP00000456117.1:p.Pro263Thr | |
| ENST00000565778.6:c.418C>A | ENSP00000458015.1:p.Pro140Thr | |
| ENST00000566083.6:n.1245C>A | ||
| ENST00000566824.6:n.767C>A | ||
| ENST00000567963.6:c.625C>A | ENSP00000455387.2:p.Pro209Thr | |
| ENST00000568076.6:n.914C>A | ||
| ENST00000568422.6:c.*24C>A | ENSP00000455549.2:n.*24C>A | |
| ENST00000568452.6:n.890C>A | ||
| ENST00000568472.6:n.663C>A | ||
| ENST00000568497.6:c.-183C>A | ENSP00000456414.2:n.-183C>A | |
| ENST00000568558.6:c.490C>A | ENSP00000455603.2:p.Pro164Thr | |
| ENST00000569430.7:c.787C>A | ENSP00000454229.1:p.Pro263Thr | |
| ENST00000628023.3:c.*83C>A | ENSP00000486178.1:n.*83C>A | |
| ENST00000635861.1:c.*311C>A | ENSP00000490034.1:n.*311C>A | |
| ENST00000635887.1:c.787C>A | ENSP00000490709.1:p.Pro263Thr | |
| ENST00000635958.1:n.898C>A | ||
| ENST00000635973.1:c.538C>A | ENSP00000490363.1:p.Pro180Thr | |
| ENST00000636017.1:c.*311C>A | ENSP00000490538.1:n.*311C>A | |
| ENST00000636078.1:n.829C>A | ||
| ENST00000636147.2:c.787C>A MANE Select | ENSP00000490105.1:p.Pro263Thr | |
| ENST00000636172.1:c.*311C>A | ENSP00000490505.1:n.*311C>A | |
| ENST00000636228.1:c.481C>A | ENSP00000489627.1:p.Pro161Thr | |
| ENST00000636351.1:n.507C>A | ||
| ENST00000636503.1:c.787C>A | ENSP00000489824.1:p.Pro263Thr | |
| ENST00000636685.1:n.294C>A | ||
| ENST00000636766.1:c.787C>A | ENSP00000489841.1:p.Pro263Thr | |
| ENST00000636839.1:n.939C>A | ||
| ENST00000636853.1:n.1702C>A | ||
| ENST00000636866.1:c.787C>A | ENSP00000490880.1:p.Pro263Thr | |
| ENST00000636907.1:n.938C>A | ||
| ENST00000636977.1:n.1855C>A | ||
| ENST00000637050.1:n.874C>A | ||
| ENST00000637100.1:c.787C>A | ENSP00000490394.1:p.Pro263Thr | |
| ENST00000637107.1:c.*311C>A | ENSP00000490248.1:n.*311C>A | |
| ENST00000637184.1:c.787C>A | ENSP00000489952.1:p.Pro263Thr | |
| ENST00000637299.1:c.*596C>A | ENSP00000489823.1:n.*596C>A | |
| ENST00000637376.1:c.787C>A | ENSP00000490758.1:p.Pro263Thr | |
| ENST00000637578.1:c.*311C>A | ENSP00000490206.1:n.*311C>A | |
| ENST00000637699.1:c.570C>A | ENSP00000490049.1:n.570C>A | |
| ENST00000637745.1:c.126C>A | ||
| ENST00000637871.1:c.*311C>A | ENSP00000490670.1:n.*311C>A | |
| ENST00000333496.13:c.715C>A | ENSP00000329171.9:p.Pro239Thr | |
| ENST00000355477.9:c.*24C>A | ENSP00000347660.6:n.*24C>A | |
| ENST00000357806.11:c.490C>A | ENSP00000350457.7:p.Pro164Thr | |
| ENST00000357857.13:c.625C>A | ENSP00000350523.9:p.Pro209Thr | |
| ENST00000359984.11:c.481C>A | ENSP00000353073.8:p.Pro161Thr | |
| ENST00000360019.6:c.787C>A | ENSP00000353116.2:p.Pro263Thr | |
| ENST00000395653.8:c.487C>A | ENSP00000379014.4:p.Pro163Thr | |
| ENST00000561689.5:n.628C>A | ||
| ENST00000563874.5:n.2141C>A | ||
| ENST00000564574.5:n.835C>A | ||
| ENST00000565047.1:n.381C>A | ||
| ENST00000565140.5:c.570C>A | ENSP00000455342.1:n.570C>A | |
| ENST00000565316.5:c.787C>A | ENSP00000456117.1:p.Pro263Thr | |
| ENST00000565354.5:n.6C>A | ||
| ENST00000565778.5:c.418C>A | ENSP00000458015.1:p.Pro140Thr | |
| ENST00000566057.5:c.401C>A | ENSP00000456693.1:n.401C>A | |
| ENST00000566083.5:n.1018C>A | ||
| ENST00000566824.5:n.836C>A | ||
| ENST00000567495.5:c.*24C>A | ENSP00000456013.1:n.*24C>A | |
| ENST00000567963.5:c.787C>A | ENSP00000455387.1:p.Pro263Thr | |
| ENST00000568076.5:n.570C>A | ||
| ENST00000568224.4:c.553C>A | ENSP00000454253.1:p.Pro185Thr | |
| ENST00000568422.5:c.*24C>A | ENSP00000455549.1:n.*24C>A | |
| ENST00000568452.5:n.787C>A | ||
| ENST00000568472.5:n.267C>A | ||
| ENST00000568497.5:c.*83C>A | ENSP00000456414.1:n.*83C>A | |
| ENST00000568558.5:c.328C>A | ENSP00000455603.1:p.Pro110Thr | |
| ENST00000569030.5:c.461-1337C>A | ENSP00000454680.1:n.461-1337C>A | |
| ENST00000569430.5:c.787C>A | ENSP00000454229.1:p.Pro263Thr | |
| ENST00000628023.2:c.*83C>A | ENSP00000486178.1:n.*83C>A | |
| ENST00000631023.2:c.787C>A | ENSP00000486616.1:p.Pro263Thr | |
| NM_000086.2:c.787C>A , LRG_689t1:c.787C>A | NP_000077.1:p.Pro263Thr | |
| NM_001042432.1:c.787C>A , LRG_689t2:c.787C>A | NP_001035897.1:p.Pro263Thr | |
| NM_001286104.1:c.715C>A | NP_001273033.1:p.Pro239Thr | |
| NM_001286105.1:c.487C>A | NP_001273034.1:p.Pro163Thr | |
| NM_001286109.1:c.553C>A | NP_001273038.1:p.Pro185Thr | |
| NM_001286110.1:c.625C>A | NP_001273039.1:p.Pro209Thr | |
| NM_001042432.2:c.787C>A MANE Select | NP_001035897.1:p.Pro263Thr | |
| NM_001286104.2:c.715C>A | NP_001273033.1:p.Pro239Thr | |
| NM_001286105.2:c.487C>A | NP_001273034.1:p.Pro163Thr | |
| NM_001286109.2:c.553C>A | NP_001273038.1:p.Pro185Thr | |
| NM_001286110.2:c.625C>A | NP_001273039.1:p.Pro209Thr |