Linked Data
ClinVar Variation Id:
389901
dbSNP Id:
rs371648038
ExAC:
X:31496274 G / A
gnomAD v2:
X-31496274-G-A
gnomAD v3:
X-31478157-G-A
gnomAD v4:
X-31478157-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31478157G>A , CM000685.2:g.31478157G>A | GRCh38 |
| NC_000023.10:g.31496274G>A , CM000685.1:g.31496274G>A | GRCh37 |
| NC_000023.9:g.31406195G>A | NCBI36 |
| NG_012232.1:g.1866453C>T , LRG_199:g.1866453C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.3732C>T | ENSP00000350765.3:p.Pro1244= | |
| ENST00000682238.1:c.1506C>T | ENSP00000508124.1:p.Pro502= | |
| ENST00000683450.1:n.2351C>T | ||
| ENST00000683957.1:n.2378C>T | ||
| ENST00000684130.1:c.1506C>T | ENSP00000508037.1:p.Pro502= | |
| ENST00000343523.7:c.741C>T | ENSP00000340057.4:p.Pro247= | |
| ENST00000357033.9:c.8886C>T MANE Select | ENSP00000354923.3:p.Pro2962= | |
| ENST00000619831.5:c.4854C>T | ENSP00000479270.2:p.Pro1618= | |
| ENST00000620040.5:c.1506C>T | ENSP00000478150.2:p.Pro502= | |
| ENST00000680961.1:c.1506C>T | ENSP00000506386.1:p.Pro502= | |
| ENST00000681646.1:n.2547C>T | ||
| ENST00000343523.6:c.699C>T | ENSP00000340057.3:p.Pro233= | |
| ENST00000357033.8:c.8886C>T | ENSP00000354923.3:p.Pro2962= | |
| ENST00000358062.6:c.1974C>T | ENSP00000350765.2:p.Pro658= | |
| ENST00000359836.5:c.1506C>T | ENSP00000352894.1:p.Pro502= | |
| ENST00000378677.6:c.8874C>T | ENSP00000367948.2:p.Pro2958= | |
| ENST00000378707.7:c.1506C>T | ENSP00000367979.3:p.Pro502= | |
| ENST00000474231.5:c.1506C>T | ENSP00000417123.1:p.Pro502= | |
| ENST00000541735.5:c.1506C>T | ENSP00000444119.1:p.Pro502= | |
| ENST00000619831.4:c.8871C>T | ENSP00000479270.1:p.Pro2957= | |
| ENST00000620040.4:c.8883C>T | ENSP00000478150.1:p.Pro2961= | |
| NM_000109.3:c.8862C>T | NP_000100.2:p.Pro2954= | |
| NM_004006.2:c.8886C>T , LRG_199t1:c.8886C>T | NP_003997.1:p.Pro2962= | |
| NM_004009.3:c.8874C>T | NP_004000.1:p.Pro2958= | |
| NM_004010.3:c.8517C>T | NP_004001.1:p.Pro2839= | |
| NM_004011.3:c.4863C>T | NP_004002.2:p.Pro1621= | |
| NM_004012.3:c.4854C>T | NP_004003.1:p.Pro1618= | |
| NM_004013.2:c.1506C>T | NP_004004.1:p.Pro502= | |
| NM_004014.2:c.699C>T | NP_004005.1:p.Pro233= | |
| NM_004020.3:c.1506C>T | NP_004011.2:p.Pro502= | |
| NM_004021.2:c.1506C>T | NP_004012.1:p.Pro502= | |
| NM_004022.2:c.1506C>T | NP_004013.1:p.Pro502= | |
| NM_004023.2:c.1506C>T | NP_004014.1:p.Pro502= | |
| XM_006724468.2:c.8886C>T | XP_006724531.1:p.Pro2962= | |
| XM_006724469.2:c.8862C>T | XP_006724532.1:p.Pro2954= | |
| XM_006724470.2:c.8886C>T | XP_006724533.1:p.Pro2962= | |
| XM_006724471.2:c.8886C>T | XP_006724534.1:p.Pro2962= | |
| XM_006724472.2:c.8757C>T | XP_006724535.1:p.Pro2919= | |
| XM_006724473.2:c.8748C>T | XP_006724536.1:p.Pro2916= | |
| XM_006724474.2:c.8886C>T | XP_006724537.1:p.Pro2962= | |
| XM_006724475.2:c.8886C>T | XP_006724538.1:p.Pro2962= | |
| XM_011545467.1:c.8763C>T | XP_011543769.1:p.Pro2921= | |
| XM_011545468.1:c.8886C>T | XP_011543770.1:p.Pro2962= | |
| XM_006724469.3:c.8862C>T | XP_006724532.1:p.Pro2954= | |
| XM_006724470.3:c.8886C>T | XP_006724533.1:p.Pro2962= | |
| XM_006724474.3:c.8886C>T | XP_006724537.1:p.Pro2962= | |
| XM_011545468.2:c.8886C>T | XP_011543770.1:p.Pro2962= | |
| XM_017029328.1:c.8886C>T | XP_016884817.1:p.Pro2962= | |
| XM_017029331.1:c.3060C>T | XP_016884820.1:p.Pro1020= | |
| NM_000109.4:c.8862C>T | NP_000100.3:p.Pro2954= | |
| NM_004006.3:c.8886C>T MANE Select | NP_003997.2:p.Pro2962= | |
| NM_004011.4:c.4863C>T | NP_004002.3:p.Pro1621= | |
| NM_004012.4:c.4854C>T | NP_004003.2:p.Pro1618= | |
| NM_004021.3:c.1506C>T | NP_004012.2:p.Pro502= | |
| NM_004023.3:c.1506C>T | NP_004014.2:p.Pro502= | |
| NM_004013.3:c.1506C>T | NP_004004.2:p.Pro502= | |
| NM_004014.3:c.699C>T | NP_004005.2:p.Pro233= | |
| NM_004020.4:c.1506C>T | NP_004011.3:p.Pro502= | |
| NM_004022.3:c.1506C>T | NP_004013.2:p.Pro502= |