Linked Data
ClinVar Variation Id:
409922
dbSNP Id:
rs772732788
ExAC:
X:31525549 C / T
gnomAD v2:
X-31525549-C-T
gnomAD v4:
X-31507432-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31507432C>T , CM000685.2:g.31507432C>T | GRCh38 |
| NC_000023.10:g.31525549C>T , CM000685.1:g.31525549C>T | GRCh37 |
| NC_000023.9:g.31435470C>T | NCBI36 |
| NG_012232.1:g.1837178G>A , LRG_199:g.1837178G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.3085G>A | ENSP00000350765.3:p.Ala1029Thr | |
| ENST00000682238.1:c.859G>A | ENSP00000508124.1:p.Ala287Thr | |
| ENST00000683450.1:n.1704G>A | ||
| ENST00000683957.1:n.1731G>A | ||
| ENST00000684130.1:c.859G>A | ENSP00000508037.1:p.Ala287Thr | |
| ENST00000343523.7:c.94G>A | ENSP00000340057.4:p.Ala32Thr | |
| ENST00000357033.9:c.8239G>A MANE Select | ENSP00000354923.3:p.Ala2747Thr | |
| ENST00000619831.5:c.4207G>A | ENSP00000479270.2:p.Ala1403Thr | |
| ENST00000620040.5:c.859G>A | ENSP00000478150.2:p.Ala287Thr | |
| ENST00000680961.1:c.859G>A | ENSP00000506386.1:p.Ala287Thr | |
| ENST00000681646.1:n.1900G>A | ||
| ENST00000343523.6:c.52G>A | ENSP00000340057.3:p.Ala18Thr | |
| ENST00000357033.8:c.8239G>A | ENSP00000354923.3:p.Ala2747Thr | |
| ENST00000358062.6:c.1327G>A | ENSP00000350765.2:p.Ala443Thr | |
| ENST00000359836.5:c.859G>A | ENSP00000352894.1:p.Ala287Thr | |
| ENST00000378677.6:c.8227G>A | ENSP00000367948.2:p.Ala2743Thr | |
| ENST00000378707.7:c.859G>A | ENSP00000367979.3:p.Ala287Thr | |
| ENST00000445312.1:n.296G>A | ||
| ENST00000474231.5:c.859G>A | ENSP00000417123.1:p.Ala287Thr | |
| ENST00000541735.5:c.859G>A | ENSP00000444119.1:p.Ala287Thr | |
| ENST00000619831.4:c.8224G>A | ENSP00000479270.1:p.Ala2742Thr | |
| ENST00000620040.4:c.8236G>A | ENSP00000478150.1:p.Ala2746Thr | |
| NM_000109.3:c.8215G>A | NP_000100.2:p.Ala2739Thr | |
| NM_004006.2:c.8239G>A , LRG_199t1:c.8239G>A | NP_003997.1:p.Ala2747Thr | |
| NM_004009.3:c.8227G>A | NP_004000.1:p.Ala2743Thr | |
| NM_004010.3:c.7870G>A | NP_004001.1:p.Ala2624Thr | |
| NM_004011.3:c.4216G>A | NP_004002.2:p.Ala1406Thr | |
| NM_004012.3:c.4207G>A | NP_004003.1:p.Ala1403Thr | |
| NM_004013.2:c.859G>A | NP_004004.1:p.Ala287Thr | |
| NM_004014.2:c.52G>A | NP_004005.1:p.Ala18Thr | |
| NM_004020.3:c.859G>A | NP_004011.2:p.Ala287Thr | |
| NM_004021.2:c.859G>A | NP_004012.1:p.Ala287Thr | |
| NM_004022.2:c.859G>A | NP_004013.1:p.Ala287Thr | |
| NM_004023.2:c.859G>A | NP_004014.1:p.Ala287Thr | |
| XM_006724468.2:c.8239G>A | XP_006724531.1:p.Ala2747Thr | |
| XM_006724469.2:c.8215G>A | XP_006724532.1:p.Ala2739Thr | |
| XM_006724470.2:c.8239G>A | XP_006724533.1:p.Ala2747Thr | |
| XM_006724471.2:c.8239G>A | XP_006724534.1:p.Ala2747Thr | |
| XM_006724472.2:c.8110G>A | XP_006724535.1:p.Ala2704Thr | |
| XM_006724473.2:c.8101G>A | XP_006724536.1:p.Ala2701Thr | |
| XM_006724474.2:c.8239G>A | XP_006724537.1:p.Ala2747Thr | |
| XM_006724475.2:c.8239G>A | XP_006724538.1:p.Ala2747Thr | |
| XM_011545467.1:c.8116G>A | XP_011543769.1:p.Ala2706Thr | |
| XM_011545468.1:c.8239G>A | XP_011543770.1:p.Ala2747Thr | |
| XM_006724469.3:c.8215G>A | XP_006724532.1:p.Ala2739Thr | |
| XM_006724470.3:c.8239G>A | XP_006724533.1:p.Ala2747Thr | |
| XM_006724474.3:c.8239G>A | XP_006724537.1:p.Ala2747Thr | |
| XM_011545468.2:c.8239G>A | XP_011543770.1:p.Ala2747Thr | |
| XM_017029328.1:c.8239G>A | XP_016884817.1:p.Ala2747Thr | |
| XM_017029331.1:c.2413G>A | XP_016884820.1:p.Ala805Thr | |
| NM_000109.4:c.8215G>A | NP_000100.3:p.Ala2739Thr | |
| NM_004006.3:c.8239G>A MANE Select | NP_003997.2:p.Ala2747Thr | |
| NM_004011.4:c.4216G>A | NP_004002.3:p.Ala1406Thr | |
| NM_004012.4:c.4207G>A | NP_004003.2:p.Ala1403Thr | |
| NM_004021.3:c.859G>A | NP_004012.2:p.Ala287Thr | |
| NM_004023.3:c.859G>A | NP_004014.2:p.Ala287Thr | |
| NM_004013.3:c.859G>A | NP_004004.2:p.Ala287Thr | |
| NM_004014.3:c.52G>A | NP_004005.2:p.Ala18Thr | |
| NM_004020.4:c.859G>A | NP_004011.3:p.Ala287Thr | |
| NM_004022.3:c.859G>A | NP_004013.2:p.Ala287Thr |