Linked Data
ClinVar Variation Id:
287815
dbSNP Id:
rs754997935
ExAC:
X:31676220 A / G
gnomAD v2:
X-31676220-A-G
gnomAD v3:
X-31658103-A-G
gnomAD v4:
X-31658103-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31658103A>G , CM000685.2:g.31658103A>G | GRCh38 |
| NC_000023.10:g.31676220A>G , CM000685.1:g.31676220A>G | GRCh37 |
| NC_000023.9:g.31586141A>G | NCBI36 |
| NG_012232.1:g.1686507T>C , LRG_199:g.1686507T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.2760T>C | ENSP00000350765.3:p.Asp920= | |
| ENST00000682238.1:c.534T>C | ENSP00000508124.1:p.Asp178= | |
| ENST00000683450.1:n.1379T>C | ||
| ENST00000683851.1:n.1575T>C | ||
| ENST00000683957.1:n.1406T>C | ||
| ENST00000684130.1:c.534T>C | ENSP00000508037.1:p.Asp178= | |
| ENST00000357033.9:c.7914T>C MANE Select | ENSP00000354923.3:p.Asp2638= | |
| ENST00000619831.5:c.3882T>C | ENSP00000479270.2:p.Asp1294= | |
| ENST00000620040.5:c.534T>C | ENSP00000478150.2:p.Asp178= | |
| ENST00000680961.1:c.534T>C | ENSP00000506386.1:p.Asp178= | |
| ENST00000681646.1:n.1575T>C | ||
| ENST00000357033.8:c.7914T>C | ENSP00000354923.3:p.Asp2638= | |
| ENST00000358062.6:c.1002T>C | ENSP00000350765.2:p.Asp334= | |
| ENST00000359836.5:c.534T>C | ENSP00000352894.1:p.Asp178= | |
| ENST00000378677.6:c.7902T>C | ENSP00000367948.2:p.Asp2634= | |
| ENST00000378707.7:c.534T>C | ENSP00000367979.3:p.Asp178= | |
| ENST00000474231.5:c.534T>C | ENSP00000417123.1:p.Asp178= | |
| ENST00000541735.5:c.534T>C | ENSP00000444119.1:p.Asp178= | |
| ENST00000619831.4:c.7899T>C | ENSP00000479270.1:p.Asp2633= | |
| ENST00000620040.4:c.7911T>C | ENSP00000478150.1:p.Asp2637= | |
| NM_000109.3:c.7890T>C | NP_000100.2:p.Asp2630= | |
| NM_004006.2:c.7914T>C , LRG_199t1:c.7914T>C | NP_003997.1:p.Asp2638= | |
| NM_004009.3:c.7902T>C | NP_004000.1:p.Asp2634= | |
| NM_004010.3:c.7545T>C | NP_004001.1:p.Asp2515= | |
| NM_004011.3:c.3891T>C | NP_004002.2:p.Asp1297= | |
| NM_004012.3:c.3882T>C | NP_004003.1:p.Asp1294= | |
| NM_004013.2:c.534T>C | NP_004004.1:p.Asp178= | |
| NM_004020.3:c.534T>C | NP_004011.2:p.Asp178= | |
| NM_004021.2:c.534T>C | NP_004012.1:p.Asp178= | |
| NM_004022.2:c.534T>C | NP_004013.1:p.Asp178= | |
| NM_004023.2:c.534T>C | NP_004014.1:p.Asp178= | |
| XM_006724468.2:c.7914T>C | XP_006724531.1:p.Asp2638= | |
| XM_006724469.2:c.7890T>C | XP_006724532.1:p.Asp2630= | |
| XM_006724470.2:c.7914T>C | XP_006724533.1:p.Asp2638= | |
| XM_006724471.2:c.7914T>C | XP_006724534.1:p.Asp2638= | |
| XM_006724472.2:c.7785T>C | XP_006724535.1:p.Asp2595= | |
| XM_006724473.2:c.7776T>C | XP_006724536.1:p.Asp2592= | |
| XM_006724474.2:c.7914T>C | XP_006724537.1:p.Asp2638= | |
| XM_006724475.2:c.7914T>C | XP_006724538.1:p.Asp2638= | |
| XM_011545467.1:c.7791T>C | XP_011543769.1:p.Asp2597= | |
| XM_011545468.1:c.7914T>C | XP_011543770.1:p.Asp2638= | |
| XM_006724469.3:c.7890T>C | XP_006724532.1:p.Asp2630= | |
| XM_006724470.3:c.7914T>C | XP_006724533.1:p.Asp2638= | |
| XM_006724474.3:c.7914T>C | XP_006724537.1:p.Asp2638= | |
| XM_011545468.2:c.7914T>C | XP_011543770.1:p.Asp2638= | |
| XM_017029328.1:c.7914T>C | XP_016884817.1:p.Asp2638= | |
| XM_017029331.1:c.2088T>C | XP_016884820.1:p.Asp696= | |
| NM_000109.4:c.7890T>C | NP_000100.3:p.Asp2630= | |
| NM_004006.3:c.7914T>C MANE Select | NP_003997.2:p.Asp2638= | |
| NM_004011.4:c.3891T>C | NP_004002.3:p.Asp1297= | |
| NM_004012.4:c.3882T>C | NP_004003.2:p.Asp1294= | |
| NM_004021.3:c.534T>C | NP_004012.2:p.Asp178= | |
| NM_004023.3:c.534T>C | NP_004014.2:p.Asp178= | |
| NM_004013.3:c.534T>C | NP_004004.2:p.Asp178= | |
| NM_004020.4:c.534T>C | NP_004011.3:p.Asp178= | |
| NM_004022.3:c.534T>C | NP_004013.2:p.Asp178= |