Linked Data
dbSNP Id:
rs72542747
ExAC:
5:142680287 T / A
gnomAD v2:
5-142680287-T-A
gnomAD v3:
5-143300722-T-A
gnomAD v4:
5-143300722-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.143300722T>A , CM000667.2:g.143300722T>A | GRCh38 |
| NC_000005.9:g.142680287T>A , CM000667.1:g.142680287T>A | GRCh37 |
| NC_000005.8:g.142660480T>A | NCBI36 |
| NG_009062.1:g.139791A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394464.7:c.1510A>T MANE Select | ENSP00000377977.2:p.Thr504Ser | |
| ENST00000652686.1:c.1510A>T | ENSP00000498663.1:p.Thr504Ser | |
| ENST00000231509.7:c.1513A>T | ENSP00000231509.3:p.Thr505Ser | |
| ENST00000343796.6:c.1510A>T | ENSP00000343205.2:p.Thr504Ser | |
| ENST00000394464.6:c.1510A>T | ENSP00000377977.2:p.Thr504Ser | |
| ENST00000394466.6:c.1513A>T | ENSP00000377979.2:p.Thr505Ser | |
| ENST00000415690.6:c.1510A>T | ENSP00000387672.2:p.Thr504Ser | |
| ENST00000424646.6:c.1432A>T | ENSP00000405282.2:p.Thr478Ser | |
| ENST00000503201.1:c.1510A>T | ENSP00000427672.1:p.Thr504Ser | |
| ENST00000504336.1:n.450A>T | ||
| ENST00000504572.5:c.1513A>T | ENSP00000422518.1:p.Thr505Ser | |
| NM_000176.2:c.1510A>T | NP_000167.1:p.Thr504Ser | |
| NM_001018074.1:c.1510A>T | NP_001018084.1:p.Thr504Ser | |
| NM_001018075.1:c.1510A>T | NP_001018085.1:p.Thr504Ser | |
| NM_001018076.1:c.1510A>T | NP_001018086.1:p.Thr504Ser | |
| NM_001018077.1:c.1510A>T | NP_001018087.1:p.Thr504Ser | |
| NM_001020825.1:c.1510A>T | NP_001018661.1:p.Thr504Ser | |
| NM_001024094.1:c.1513A>T | NP_001019265.1:p.Thr505Ser | |
| NM_001204258.1:c.1432A>T | NP_001191187.1:p.Thr478Ser | |
| NM_001204259.1:c.1255A>T | NP_001191188.1:p.Thr419Ser | |
| NM_001204260.1:c.1243A>T | NP_001191189.1:p.Thr415Ser | |
| NM_001204261.1:c.1219A>T | NP_001191190.1:p.Thr407Ser | |
| NM_001204262.1:c.565A>T | NP_001191191.1:p.Thr189Ser | |
| NM_001204263.1:c.520A>T | NP_001191192.1:p.Thr174Ser | |
| NM_001204264.1:c.505A>T | NP_001191193.1:p.Thr169Ser | |
| NM_001204265.1:c.1510A>T | NP_001191194.1:p.Thr504Ser | |
| XM_005268419.2:c.1513A>T | XP_005268476.1:p.Thr505Ser | |
| XM_005268420.3:c.1513A>T | XP_005268477.1:p.Thr505Ser | |
| XM_005268422.2:c.1513A>T | XP_005268479.1:p.Thr505Ser | |
| XM_005268423.2:c.1513A>T | XP_005268480.1:p.Thr505Ser | |
| XM_011537637.1:c.319A>T | XP_011535939.1:p.Thr107Ser | |
| NR_157096.1:n.433A>T | ||
| XM_005268419.4:c.1513A>T | XP_005268476.1:p.Thr505Ser | |
| XM_005268420.4:c.1513A>T | XP_005268477.1:p.Thr505Ser | |
| XM_005268422.3:c.1513A>T | XP_005268479.1:p.Thr505Ser | |
| XM_005268423.3:c.1513A>T | XP_005268480.1:p.Thr505Ser | |
| XM_011537637.3:c.319A>T | XP_011535939.1:p.Thr107Ser | |
| XM_017009397.1:c.1510A>T | XP_016864886.1:p.Thr504Ser | |
| XM_017009398.1:c.1510A>T | XP_016864887.1:p.Thr504Ser | |
| NM_000176.3:c.1510A>T MANE Select | NP_000167.1:p.Thr504Ser | |
| NM_001364180.1:c.1510A>T | NP_001351109.1:p.Thr504Ser | |
| NM_001364181.1:c.1510A>T | NP_001351110.1:p.Thr504Ser | |
| NM_001364182.1:c.1510A>T | NP_001351111.1:p.Thr504Ser | |
| NM_001364183.1:c.1513A>T | NP_001351112.1:p.Thr505Ser | |
| NM_001364184.1:c.1513A>T | NP_001351113.1:p.Thr505Ser | |
| NM_001364185.1:c.1513A>T | NP_001351114.1:p.Thr505Ser | |
| NM_001018076.2:c.1510A>T | NP_001018086.1:p.Thr504Ser | |
| NM_001020825.2:c.1510A>T | NP_001018661.1:p.Thr504Ser | |
| NM_001024094.2:c.1513A>T | NP_001019265.1:p.Thr505Ser | |
| NM_001204258.2:c.1432A>T | NP_001191187.1:p.Thr478Ser | |
| NM_001204259.2:c.1255A>T | NP_001191188.1:p.Thr419Ser | |
| NM_001204260.2:c.1243A>T | NP_001191189.1:p.Thr415Ser | |
| NM_001204261.2:c.1219A>T | NP_001191190.1:p.Thr407Ser | |
| NM_001204262.2:c.565A>T | NP_001191191.1:p.Thr189Ser | |
| NM_001204263.2:c.520A>T | NP_001191192.1:p.Thr174Ser | |
| NM_001204264.2:c.505A>T | NP_001191193.1:p.Thr169Ser | |
| NM_001204265.2:c.1510A>T | NP_001191194.1:p.Thr504Ser | |
| NM_001364180.2:c.1510A>T | NP_001351109.1:p.Thr504Ser | |
| NM_001364181.2:c.1510A>T | NP_001351110.1:p.Thr504Ser | |
| NM_001364183.2:c.1513A>T | NP_001351112.1:p.Thr505Ser | |
| NM_001364184.2:c.1513A>T | NP_001351113.1:p.Thr505Ser | |
| NR_157096.2:n.433A>T |