Linked Data
ClinVar Variation Id:
290614
dbSNP Id:
rs146543659
ExAC:
X:31200941 G / A
gnomAD v2:
X-31200941-G-A
gnomAD v3:
X-31182824-G-A
gnomAD v4:
X-31182824-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31182824G>A , CM000685.2:g.31182824G>A | GRCh38 |
| NC_000023.10:g.31200941G>A , CM000685.1:g.31200941G>A | GRCh37 |
| NC_000023.9:g.31110862G>A | NCBI36 |
| NG_012232.1:g.2161786C>T , LRG_199:g.2161786C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.4734C>T | ENSP00000350765.3:p.Pro1578= | |
| ENST00000680162.2:c.684C>T | ENSP00000506634.2:p.Pro228= | |
| ENST00000680768.2:c.684C>T | ENSP00000506359.2:p.Pro228= | |
| ENST00000681989.1:n.686C>T | ||
| ENST00000682238.1:c.2508C>T | ENSP00000508124.1:p.Pro836= | |
| ENST00000682322.1:c.684C>T | ENSP00000507690.1:p.Pro228= | |
| ENST00000682600.1:c.684C>T | ENSP00000507640.1:p.Pro228= | |
| ENST00000682769.1:n.606-2343C>T | ||
| ENST00000683509.1:n.1405C>T | ||
| ENST00000683675.1:n.987C>T | ||
| ENST00000683709.1:n.1406C>T | ||
| ENST00000683957.1:n.3380C>T | ||
| ENST00000684130.1:c.2508C>T | ENSP00000508037.1:p.Pro836= | |
| ENST00000343523.7:c.1743C>T | ENSP00000340057.4:p.Pro581= | |
| ENST00000357033.9:c.9888C>T MANE Select | ENSP00000354923.3:p.Pro3296= | |
| ENST00000475732.2:n.254C>T | ||
| ENST00000619831.5:c.5856C>T | ENSP00000479270.2:p.Pro1952= | |
| ENST00000620040.5:c.2508C>T | ENSP00000478150.2:p.Pro836= | |
| ENST00000679641.1:c.604-2343C>T | ENSP00000506135.1:n.604-2343C>T | |
| ENST00000680162.1:c.561C>T | ENSP00000506634.1:p.Pro187= | |
| ENST00000680355.1:c.684C>T | ENSP00000506257.1:p.Pro228= | |
| ENST00000680557.1:c.603+21137C>T | ENSP00000505164.1:n.603+21137C>T | |
| ENST00000680768.1:c.627C>T | ENSP00000506359.1:p.Pro209= | |
| ENST00000680961.1:c.2428-2343C>T | ENSP00000506386.1:n.2428-2343C>T | |
| ENST00000681153.1:c.684C>T | ENSP00000505124.1:p.Pro228= | |
| ENST00000681654.1:n.818C>T | ||
| ENST00000343523.6:c.1701C>T | ENSP00000340057.3:p.Pro567= | |
| ENST00000357033.8:c.9888C>T | ENSP00000354923.3:p.Pro3296= | |
| ENST00000358062.6:c.2976C>T | ENSP00000350765.2:p.Pro992= | |
| ENST00000359836.5:c.2508C>T | ENSP00000352894.1:p.Pro836= | |
| ENST00000361471.8:c.684C>T | ENSP00000354464.4:p.Pro228= | |
| ENST00000378677.6:c.9876C>T | ENSP00000367948.2:p.Pro3292= | |
| ENST00000378680.6:c.684C>T | ENSP00000367951.2:p.Pro228= | |
| ENST00000378702.8:c.684C>T | ENSP00000367974.4:p.Pro228= | |
| ENST00000378705.3:c.258C>T | ENSP00000367977.3:p.Pro86= | |
| ENST00000378707.7:c.2508C>T | ENSP00000367979.3:p.Pro836= | |
| ENST00000378723.7:c.684C>T | ENSP00000367997.3:p.Pro228= | |
| ENST00000474231.5:c.2508C>T | ENSP00000417123.1:p.Pro836= | |
| ENST00000475732.1:n.104C>T | ||
| ENST00000541735.5:c.2508C>T | ENSP00000444119.1:p.Pro836= | |
| ENST00000619831.4:c.9873C>T | ENSP00000479270.1:p.Pro3291= | |
| ENST00000620040.4:c.9885C>T | ENSP00000478150.1:p.Pro3295= | |
| NM_000109.3:c.9864C>T | NP_000100.2:p.Pro3288= | |
| NM_004006.2:c.9888C>T , LRG_199t1:c.9888C>T | NP_003997.1:p.Pro3296= | |
| NM_004009.3:c.9876C>T | NP_004000.1:p.Pro3292= | |
| NM_004010.3:c.9519C>T | NP_004001.1:p.Pro3173= | |
| NM_004011.3:c.5865C>T | NP_004002.2:p.Pro1955= | |
| NM_004012.3:c.5856C>T | NP_004003.1:p.Pro1952= | |
| NM_004013.2:c.2508C>T | NP_004004.1:p.Pro836= | |
| NM_004014.2:c.1701C>T | NP_004005.1:p.Pro567= | |
| NM_004015.2:c.684C>T | NP_004006.1:p.Pro228= | |
| NM_004016.2:c.684C>T | NP_004007.1:p.Pro228= | |
| NM_004017.2:c.684C>T | NP_004008.1:p.Pro228= | |
| NM_004018.2:c.684C>T | NP_004009.1:p.Pro228= | |
| NM_004019.2:c.684C>T | NP_004010.1:p.Pro228= | |
| NM_004020.3:c.2508C>T | NP_004011.2:p.Pro836= | |
| NM_004021.2:c.2508C>T | NP_004012.1:p.Pro836= | |
| NM_004022.2:c.2508C>T | NP_004013.1:p.Pro836= | |
| NM_004023.2:c.2508C>T | NP_004014.1:p.Pro836= | |
| XM_006724468.2:c.9888C>T | XP_006724531.1:p.Pro3296= | |
| XM_006724469.2:c.9864C>T | XP_006724532.1:p.Pro3288= | |
| XM_006724470.2:c.9888C>T | XP_006724533.1:p.Pro3296= | |
| XM_006724471.2:c.9888C>T | XP_006724534.1:p.Pro3296= | |
| XM_006724472.2:c.9759C>T | XP_006724535.1:p.Pro3253= | |
| XM_006724473.2:c.9750C>T | XP_006724536.1:p.Pro3250= | |
| XM_006724474.2:c.9888C>T | XP_006724537.1:p.Pro3296= | |
| XM_006724475.2:c.9888C>T | XP_006724538.1:p.Pro3296= | |
| XM_011545467.1:c.9765C>T | XP_011543769.1:p.Pro3255= | |
| XM_006724469.3:c.9864C>T | XP_006724532.1:p.Pro3288= | |
| XM_006724470.3:c.9888C>T | XP_006724533.1:p.Pro3296= | |
| XM_006724474.3:c.9888C>T | XP_006724537.1:p.Pro3296= | |
| XM_017029328.1:c.9888C>T | XP_016884817.1:p.Pro3296= | |
| XM_017029331.1:c.4062C>T | XP_016884820.1:p.Pro1354= | |
| NM_000109.4:c.9864C>T | NP_000100.3:p.Pro3288= | |
| NM_004006.3:c.9888C>T MANE Select | NP_003997.2:p.Pro3296= | |
| NM_004011.4:c.5865C>T | NP_004002.3:p.Pro1955= | |
| NM_004012.4:c.5856C>T | NP_004003.2:p.Pro1952= | |
| NM_004015.3:c.684C>T | NP_004006.1:p.Pro228= | |
| NM_004016.3:c.684C>T | NP_004007.1:p.Pro228= | |
| NM_004017.3:c.684C>T | NP_004008.1:p.Pro228= | |
| NM_004018.3:c.684C>T | NP_004009.1:p.Pro228= | |
| NM_004019.3:c.684C>T | NP_004010.1:p.Pro228= | |
| NM_004021.3:c.2508C>T | NP_004012.2:p.Pro836= | |
| NM_004023.3:c.2508C>T | NP_004014.2:p.Pro836= | |
| NM_004013.3:c.2508C>T | NP_004004.2:p.Pro836= | |
| NM_004014.3:c.1701C>T | NP_004005.2:p.Pro567= | |
| NM_004020.4:c.2508C>T | NP_004011.3:p.Pro836= | |
| NM_004022.3:c.2508C>T | NP_004013.2:p.Pro836= |