Linked Data
ClinVar Variation Id:
66780
ClinVar RCV Id:
RCV000057240
RCV000293812
RCV000298159
RCV000327855
RCV000259414
RCV000263024
RCV000377531
RCV000384768
RCV000536971
RCV000259097
RCV000289312
RCV000324542
RCV000355460
RCV000619516
RCV000776145
RCV001093854
RCV001098597
dbSNP Id:
rs267607603
ExAC:
1:156105904 G / A
gnomAD v2:
1-156105904-G-A
gnomAD v3:
1-156136113-G-A
gnomAD v4:
1-156136113-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156136113G>A , CM000663.2:g.156136113G>A | GRCh38 |
| NC_000001.10:g.156105904G>A , CM000663.1:g.156105904G>A | GRCh37 |
| NC_000001.9:g.154372528G>A | NCBI36 |
| NG_008692.2:g.58541G>A , LRG_254:g.58541G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.591G>A | ENSP00000426535.3:p.Glu197= | |
| ENST00000498722.3:n.381G>A | ||
| ENST00000682650.1:c.1149G>A | ENSP00000506904.1:p.Glu383= | |
| ENST00000683032.1:c.1149G>A | ENSP00000506771.1:p.Glu383= | |
| ENST00000684195.1:c.1149G>A | ENSP00000508220.1:p.Glu383= | |
| ENST00000361308.9:c.1149G>A | ENSP00000355292.6:p.Glu383= | |
| ENST00000368300.9:c.1149G>A MANE Select | ENSP00000357283.4:p.Glu383= | |
| ENST00000496738.6:n.1524G>A | ||
| ENST00000674518.1:c.*499G>A | ENSP00000502261.1:n.*499G>A | |
| ENST00000674600.1:c.*948G>A | ENSP00000501666.1:n.*948G>A | |
| ENST00000674720.1:c.1149G>A | ENSP00000502798.1:p.Glu383= | |
| ENST00000675431.1:n.842G>A | ||
| ENST00000675455.1:c.*949G>A | ENSP00000501795.1:n.*949G>A | |
| ENST00000675667.1:c.1149G>A | ENSP00000501803.1:p.Glu383= | |
| ENST00000675874.1:c.*620G>A | ENSP00000501851.1:n.*620G>A | |
| ENST00000675881.1:c.*160G>A | ENSP00000501670.1:n.*160G>A | |
| ENST00000675939.1:c.1149G>A | ENSP00000502256.1:p.Glu383= | |
| ENST00000675989.1:n.1524G>A | ||
| ENST00000676208.1:c.*160G>A | ENSP00000502468.1:n.*160G>A | |
| ENST00000676283.1:n.1524G>A | ||
| ENST00000676385.2:c.1149G>A | ENSP00000502091.1:p.Glu383= | |
| ENST00000676434.1:c.*160G>A | ENSP00000501648.1:n.*160G>A | |
| ENST00000677389.1:c.1149G>A MANE Plus Clinical | ENSP00000503633.1:p.Glu383= | |
| ENST00000347559.6:c.1149G>A | ENSP00000292304.3:p.Glu383= | |
| ENST00000361308.8:c.1149G>A | ENSP00000355292.5:p.Glu383= | |
| ENST00000368297.5:c.906G>A | ENSP00000357280.1:p.Glu302= | |
| ENST00000368298.2:n.413G>A | ||
| ENST00000368299.7:c.1149G>A | ENSP00000357282.3:p.Glu383= | |
| ENST00000368300.8:c.1149G>A | ENSP00000357283.4:p.Glu383= | |
| ENST00000368301.6:c.1149G>A | ENSP00000357284.2:p.Glu383= | |
| ENST00000448611.6:c.813G>A | ENSP00000395597.2:p.Glu271= | |
| ENST00000473598.6:c.852G>A | ENSP00000421821.1:p.Glu284= | |
| ENST00000496738.5:n.534G>A | ||
| ENST00000498722.2:n.381G>A | ||
| ENST00000508500.1:c.27G>A | ENSP00000424977.1:p.Glu9= | |
| NM_001257374.2:c.813G>A | NP_001244303.1:p.Glu271= | |
| NM_001282624.1:c.906G>A | NP_001269553.1:p.Glu302= | |
| NM_001282625.1:c.1149G>A | NP_001269554.1:p.Glu383= | |
| NM_001282626.1:c.1149G>A | NP_001269555.1:p.Glu383= | |
| NM_005572.3:c.1149G>A , LRG_254t1:c.1149G>A | NP_005563.1:p.Glu383= | |
| NM_170707.3:c.1149G>A | NP_733821.1:p.Glu383= | |
| NM_170708.3:c.1149G>A | NP_733822.1:p.Glu383= | |
| XM_011509533.1:c.813G>A | XP_011507835.1:p.Glu271= | |
| XM_011509534.1:c.525G>A | XP_011507836.1:p.Glu175= | |
| XR_921781.1:n.1438G>A | ||
| XM_011509534.2:c.525G>A | XP_011507836.1:p.Glu175= | |
| XR_921781.2:n.1436G>A | ||
| NM_170707.4:c.1149G>A MANE Select | NP_733821.1:p.Glu383= | |
| NM_001257374.3:c.813G>A | NP_001244303.1:p.Glu271= | |
| NM_001282626.2:c.1149G>A | NP_001269555.1:p.Glu383= | |
| NM_001282624.2:c.906G>A | NP_001269553.1:p.Glu302= | |
| NM_001282625.2:c.1149G>A | NP_001269554.1:p.Glu383= | |
| NM_005572.4:c.1149G>A MANE Plus Clinical | NP_005563.1:p.Glu383= | |
| NM_170708.4:c.1149G>A | NP_733822.1:p.Glu383= |