Linked Data
ClinVar Variation Id:
230429
dbSNP Id:
rs371185409
ExAC:
17:59761328 C / T
gnomAD v2:
17-59761328-C-T
gnomAD v3:
17-61683967-C-T
gnomAD v4:
17-61683967-C-T
PubMed:
PMID:25980754
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683967C>T , CM000679.2:g.61683967C>T | GRCh38 |
| NC_000017.10:g.59761328C>T , CM000679.1:g.59761328C>T | GRCh37 |
| NC_000017.9:g.57116110C>T | NCBI36 |
| NG_007409.2:g.184593G>A , LRG_300:g.184593G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.1819G>A | ||
| ENST00000682453.1:c.3079G>A | ENSP00000506943.1:p.Glu1027Lys | |
| ENST00000682477.1:c.*2505G>A | ENSP00000507075.1:n.*2505G>A | |
| ENST00000682589.1:n.8956G>A | ||
| ENST00000682755.1:c.2857G>A | ENSP00000507660.1:p.Glu953Lys | |
| ENST00000682989.1:c.*170G>A | ENSP00000507786.1:n.*170G>A | |
| ENST00000683039.1:c.3079G>A | ENSP00000508303.1:p.Glu1027Lys | |
| ENST00000683235.1:c.*494G>A | ENSP00000507646.1:n.*494G>A | |
| ENST00000683535.1:n.1209G>A | ||
| ENST00000684584.1:c.2242G>A | ENSP00000508044.1:p.Glu748Lys | |
| ENST00000684626.1:n.1325G>A | ||
| ENST00000684769.1:c.1269G>A | ENSP00000507691.1:n.1269G>A | |
| ENST00000259008.7:c.3079G>A MANE Select | ENSP00000259008.2:p.Glu1027Lys | |
| ENST00000259008.6:c.3079G>A | ENSP00000259008.2:p.Glu1027Lys | |
| NM_032043.2:c.3079G>A , LRG_300t1:c.3079G>A | NP_114432.2:p.Glu1027Lys | |
| XM_011525332.1:c.3139G>A | XP_011523634.1:p.Glu1047Lys | |
| XM_011525333.1:c.3139G>A | XP_011523635.1:p.Glu1047Lys | |
| XM_011525334.1:c.3139G>A | XP_011523636.1:p.Glu1047Lys | |
| XM_011525335.1:c.3079G>A | XP_011523637.1:p.Glu1027Lys | |
| XM_011525336.1:c.3019G>A | XP_011523638.1:p.Glu1007Lys | |
| XM_011525337.1:c.2938G>A | XP_011523639.1:p.Glu980Lys | |
| XM_011525338.1:c.2656G>A | XP_011523640.1:p.Glu886Lys | |
| XM_011525332.3:c.3139G>A | XP_011523634.1:p.Glu1047Lys | |
| XM_011525333.3:c.3139G>A | XP_011523635.1:p.Glu1047Lys | |
| XM_011525334.2:c.3139G>A | XP_011523636.1:p.Glu1047Lys | |
| XM_011525335.3:c.3079G>A | XP_011523637.1:p.Glu1027Lys | |
| XM_011525336.2:c.3019G>A | XP_011523638.1:p.Glu1007Lys | |
| XM_011525337.2:c.2938G>A | XP_011523639.1:p.Glu980Lys | |
| XM_011525338.2:c.2656G>A | XP_011523640.1:p.Glu886Lys | |
| XM_017025200.1:c.2596G>A | XP_016880689.1:p.Glu866Lys | |
| XM_017025201.1:c.2596G>A | XP_016880690.1:p.Glu866Lys | |
| XM_017025202.1:c.1225G>A | XP_016880691.1:p.Glu409Lys | |
| XM_017025203.1:c.1225G>A | XP_016880692.1:p.Glu409Lys | |
| NM_032043.3:c.3079G>A MANE Select | NP_114432.2:p.Glu1027Lys |