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
dbSNP Id:
rs1384612641
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28484116T>G , CM000678.2:g.28484116T>G | GRCh38 |
| NC_000016.9:g.28495437T>G , CM000678.1:g.28495437T>G | GRCh37 |
| NC_000016.8:g.28402938T>G | NCBI36 |
| NG_008654.2:g.13187A>C , LRG_689:g.13187A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333496.14:c.608A>C | ENSP00000329171.9:p.Tyr203Ser | |
| ENST00000355477.10:c.536A>C | ENSP00000347660.7:p.Tyr179Ser | |
| ENST00000357857.14:c.518A>C | ENSP00000350523.9:p.Tyr173Ser | |
| ENST00000359984.12:c.680A>C | ENSP00000353073.9:p.Tyr227Ser | |
| ENST00000360019.8:c.608A>C | ENSP00000353116.3:p.Tyr203Ser | |
| ENST00000395653.9:c.221A>C | ENSP00000379014.5:p.Tyr74Ser | |
| ENST00000561689.6:n.965A>C | ||
| ENST00000564091.6:c.20A>C | ENSP00000454466.2:p.Tyr7Ser | |
| ENST00000565316.6:c.680A>C | ENSP00000456117.1:p.Tyr227Ser | |
| ENST00000565778.6:c.311A>C | ENSP00000458015.1:p.Tyr104Ser | |
| ENST00000566083.6:n.1138A>C | ||
| ENST00000566824.6:n.660A>C | ||
| ENST00000567495.6:c.*139A>C | ENSP00000456013.2:n.*139A>C | |
| ENST00000567963.6:c.518A>C | ENSP00000455387.2:p.Tyr173Ser | |
| ENST00000568076.6:n.807A>C | ||
| ENST00000568422.6:c.463A>C | ENSP00000455549.2:p.Ile155Leu | |
| ENST00000568452.6:n.783A>C | ||
| ENST00000568472.6:n.556A>C | ||
| ENST00000568497.6:c.-290A>C | ENSP00000456414.2:n.-290A>C | |
| ENST00000568558.6:c.383A>C | ENSP00000455603.2:p.Tyr128Ser | |
| ENST00000569430.7:c.680A>C | ENSP00000454229.1:p.Tyr227Ser | |
| ENST00000628023.3:c.225A>C | ENSP00000486178.1:p.Leu75= | |
| ENST00000635861.1:c.*204A>C | ENSP00000490034.1:n.*204A>C | |
| ENST00000635887.1:c.680A>C | ENSP00000490709.1:p.Tyr227Ser | |
| ENST00000635958.1:n.791A>C | ||
| ENST00000635973.1:c.431A>C | ENSP00000490363.1:p.Tyr144Ser | |
| ENST00000636017.1:c.*204A>C | ENSP00000490538.1:n.*204A>C | |
| ENST00000636078.1:n.722A>C | ||
| ENST00000636147.2:c.680A>C MANE Select | ENSP00000490105.1:p.Tyr227Ser | |
| ENST00000636172.1:c.*204A>C | ENSP00000490505.1:n.*204A>C | |
| ENST00000636228.1:c.374A>C | ENSP00000489627.1:p.Tyr125Ser | |
| ENST00000636351.1:n.400A>C | ||
| ENST00000636503.1:c.680A>C | ENSP00000489824.1:p.Tyr227Ser | |
| ENST00000636685.1:n.187A>C | ||
| ENST00000636766.1:c.680A>C | ENSP00000489841.1:p.Tyr227Ser | |
| ENST00000636839.1:n.832A>C | ||
| ENST00000636853.1:n.1595A>C | ||
| ENST00000636866.1:c.680A>C | ENSP00000490880.1:p.Tyr227Ser | |
| ENST00000636907.1:n.831A>C | ||
| ENST00000636977.1:n.1748A>C | ||
| ENST00000637050.1:n.767A>C | ||
| ENST00000637100.1:c.680A>C | ENSP00000490394.1:p.Tyr227Ser | |
| ENST00000637107.1:c.*204A>C | ENSP00000490248.1:n.*204A>C | |
| ENST00000637184.1:c.680A>C | ENSP00000489952.1:p.Tyr227Ser | |
| ENST00000637299.1:c.*489A>C | ENSP00000489823.1:n.*489A>C | |
| ENST00000637376.1:c.680A>C | ENSP00000490758.1:p.Tyr227Ser | |
| ENST00000637578.1:c.*204A>C | ENSP00000490206.1:n.*204A>C | |
| ENST00000637699.1:c.463A>C | ENSP00000490049.1:p.Ile155Leu | |
| ENST00000637745.1:c.19A>C | ||
| ENST00000637871.1:c.*204A>C | ENSP00000490670.1:n.*204A>C | |
| ENST00000333496.13:c.608A>C | ENSP00000329171.9:p.Tyr203Ser | |
| ENST00000355477.9:c.463A>C | ENSP00000347660.6:p.Ile155Leu | |
| ENST00000357806.11:c.383A>C | ENSP00000350457.7:p.Tyr128Ser | |
| ENST00000357857.13:c.518A>C | ENSP00000350523.9:p.Tyr173Ser | |
| ENST00000359984.11:c.374A>C | ENSP00000353073.8:p.Tyr125Ser | |
| ENST00000360019.6:c.680A>C | ENSP00000353116.2:p.Tyr227Ser | |
| ENST00000395653.8:c.380A>C | ENSP00000379014.4:p.Tyr127Ser | |
| ENST00000561689.5:n.521A>C | ||
| ENST00000563874.5:n.2034A>C | ||
| ENST00000564574.5:n.728A>C | ||
| ENST00000565047.1:n.274A>C | ||
| ENST00000565140.5:c.463A>C | ENSP00000455342.1:p.Ile155Leu | |
| ENST00000565316.5:c.680A>C | ENSP00000456117.1:p.Tyr227Ser | |
| ENST00000565688.5:c.431A>C | ENSP00000456122.1:p.Tyr144Ser | |
| ENST00000565778.5:c.311A>C | ENSP00000458015.1:p.Tyr104Ser | |
| ENST00000566057.5:c.294A>C | ENSP00000456693.1:p.Leu98= | |
| ENST00000566083.5:n.911A>C | ||
| ENST00000566824.5:n.729A>C | ||
| ENST00000567495.5:c.463A>C | ENSP00000456013.1:p.Ile155Leu | |
| ENST00000567963.5:c.680A>C | ENSP00000455387.1:p.Tyr227Ser | |
| ENST00000568076.5:n.463A>C | ||
| ENST00000568224.4:c.446A>C | ENSP00000454253.1:p.Tyr149Ser | |
| ENST00000568422.5:c.316A>C | ENSP00000455549.1:p.Ile106Leu | |
| ENST00000568452.5:n.680A>C | ||
| ENST00000568472.5:n.160A>C | ||
| ENST00000568497.5:c.225A>C | ENSP00000456414.1:p.Leu75= | |
| ENST00000568558.5:c.221A>C | ENSP00000455603.1:p.Tyr74Ser | |
| ENST00000569030.5:c.461-1444A>C | ENSP00000454680.1:n.461-1444A>C | |
| ENST00000569430.5:c.680A>C | ENSP00000454229.1:p.Tyr227Ser | |
| ENST00000628023.2:c.225A>C | ENSP00000486178.1:p.Leu75= | |
| ENST00000631023.2:c.680A>C | ENSP00000486616.1:p.Tyr227Ser | |
| NM_000086.2:c.680A>C , LRG_689t1:c.680A>C | NP_000077.1:p.Tyr227Ser | |
| NM_001042432.1:c.680A>C , LRG_689t2:c.680A>C | NP_001035897.1:p.Tyr227Ser | |
| NM_001286104.1:c.608A>C | NP_001273033.1:p.Tyr203Ser | |
| NM_001286105.1:c.380A>C | NP_001273034.1:p.Tyr127Ser | |
| NM_001286109.1:c.446A>C | NP_001273038.1:p.Tyr149Ser | |
| NM_001286110.1:c.518A>C | NP_001273039.1:p.Tyr173Ser | |
| NM_001042432.2:c.680A>C MANE Select | NP_001035897.1:p.Tyr227Ser | |
| NM_001286104.2:c.608A>C | NP_001273033.1:p.Tyr203Ser | |
| NM_001286105.2:c.380A>C | NP_001273034.1:p.Tyr127Ser | |
| NM_001286109.2:c.446A>C | NP_001273038.1:p.Tyr149Ser | |
| NM_001286110.2:c.518A>C | NP_001273039.1:p.Tyr173Ser |