Linked Data
ClinVar Variation Id:
1467872
ClinVar RCV Id:
RCV001970509
dbSNP Id:
rs1240812601
gnomAD v3:
X-31774001-C-A
gnomAD v4:
X-31774001-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31774001C>A , CM000685.2:g.31774001C>A | GRCh38 |
| NC_000023.10:g.31792118C>A , CM000685.1:g.31792118C>A | GRCh37 |
| NC_000023.9:g.31702039C>A | NCBI36 |
| NG_012232.1:g.1570609G>T , LRG_199:g.1570609G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.2347G>T | ENSP00000350765.3:p.Gly783Cys | |
| ENST00000682238.1:c.121G>T | ENSP00000508124.1:p.Gly41Cys | |
| ENST00000683117.1:n.1162G>T | ||
| ENST00000683450.1:n.1084G>T | ||
| ENST00000683851.1:n.1162G>T | ||
| ENST00000683957.1:n.993G>T | ||
| ENST00000684130.1:c.121G>T | ENSP00000508037.1:p.Gly41Cys | |
| ENST00000357033.9:c.7501G>T MANE Select | ENSP00000354923.3:p.Gly2501Cys | |
| ENST00000619831.5:c.3469G>T | ENSP00000479270.2:p.Gly1157Cys | |
| ENST00000620040.5:c.121G>T | ENSP00000478150.2:p.Gly41Cys | |
| ENST00000680961.1:c.121G>T | ENSP00000506386.1:p.Gly41Cys | |
| ENST00000681646.1:n.1162G>T | ||
| ENST00000681839.1:c.490G>T | ENSP00000505228.1:p.Gly164Cys | |
| ENST00000357033.8:c.7501G>T | ENSP00000354923.3:p.Gly2501Cys | |
| ENST00000358062.6:c.589G>T | ENSP00000350765.2:p.Gly197Cys | |
| ENST00000359836.5:c.121G>T | ENSP00000352894.1:p.Gly41Cys | |
| ENST00000378677.6:c.7489G>T | ENSP00000367948.2:p.Gly2497Cys | |
| ENST00000378707.7:c.121G>T | ENSP00000367979.3:p.Gly41Cys | |
| ENST00000471779.1:c.258G>T | ENSP00000417075.1:n.258G>T | |
| ENST00000474231.5:c.121G>T | ENSP00000417123.1:p.Gly41Cys | |
| ENST00000541735.5:c.121G>T | ENSP00000444119.1:p.Gly41Cys | |
| ENST00000619831.4:c.7486G>T | ENSP00000479270.1:p.Gly2496Cys | |
| ENST00000620040.4:c.7498G>T | ENSP00000478150.1:p.Gly2500Cys | |
| NM_000109.3:c.7477G>T | NP_000100.2:p.Gly2493Cys | |
| NM_004006.2:c.7501G>T , LRG_199t1:c.7501G>T | NP_003997.1:p.Gly2501Cys | |
| NM_004009.3:c.7489G>T | NP_004000.1:p.Gly2497Cys | |
| NM_004010.3:c.7132G>T | NP_004001.1:p.Gly2378Cys | |
| NM_004011.3:c.3478G>T | NP_004002.2:p.Gly1160Cys | |
| NM_004012.3:c.3469G>T | NP_004003.1:p.Gly1157Cys | |
| NM_004013.2:c.121G>T | NP_004004.1:p.Gly41Cys | |
| NM_004020.3:c.121G>T | NP_004011.2:p.Gly41Cys | |
| NM_004021.2:c.121G>T | NP_004012.1:p.Gly41Cys | |
| NM_004022.2:c.121G>T | NP_004013.1:p.Gly41Cys | |
| NM_004023.2:c.121G>T | NP_004014.1:p.Gly41Cys | |
| XM_006724468.2:c.7501G>T | XP_006724531.1:p.Gly2501Cys | |
| XM_006724469.2:c.7477G>T | XP_006724532.1:p.Gly2493Cys | |
| XM_006724470.2:c.7501G>T | XP_006724533.1:p.Gly2501Cys | |
| XM_006724471.2:c.7501G>T | XP_006724534.1:p.Gly2501Cys | |
| XM_006724472.2:c.7372G>T | XP_006724535.1:p.Gly2458Cys | |
| XM_006724473.2:c.7363G>T | XP_006724536.1:p.Gly2455Cys | |
| XM_006724474.2:c.7501G>T | XP_006724537.1:p.Gly2501Cys | |
| XM_006724475.2:c.7501G>T | XP_006724538.1:p.Gly2501Cys | |
| XM_011545467.1:c.7378G>T | XP_011543769.1:p.Gly2460Cys | |
| XM_011545468.1:c.7501G>T | XP_011543770.1:p.Gly2501Cys | |
| XM_006724469.3:c.7477G>T | XP_006724532.1:p.Gly2493Cys | |
| XM_006724470.3:c.7501G>T | XP_006724533.1:p.Gly2501Cys | |
| XM_006724474.3:c.7501G>T | XP_006724537.1:p.Gly2501Cys | |
| XM_011545468.2:c.7501G>T | XP_011543770.1:p.Gly2501Cys | |
| XM_017029328.1:c.7501G>T | XP_016884817.1:p.Gly2501Cys | |
| XM_017029331.1:c.1675G>T | XP_016884820.1:p.Gly559Cys | |
| NM_000109.4:c.7477G>T | NP_000100.3:p.Gly2493Cys | |
| NM_004006.3:c.7501G>T MANE Select | NP_003997.2:p.Gly2501Cys | |
| NM_004011.4:c.3478G>T | NP_004002.3:p.Gly1160Cys | |
| NM_004012.4:c.3469G>T | NP_004003.2:p.Gly1157Cys | |
| NM_004021.3:c.121G>T | NP_004012.2:p.Gly41Cys | |
| NM_004023.3:c.121G>T | NP_004014.2:p.Gly41Cys | |
| NM_004013.3:c.121G>T | NP_004004.2:p.Gly41Cys | |
| NM_004020.4:c.121G>T | NP_004011.3:p.Gly41Cys | |
| NM_004022.3:c.121G>T | NP_004013.2:p.Gly41Cys |