Linked Data
ClinVar Variation Id:
7937
ClinVar RCV Id:
RCV000008399
dbSNP Id:
rs121909198
PubMed:
PMID:10655545
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.71244656C>T , CM000670.2:g.71244656C>T | GRCh38 |
| NC_000008.10:g.72156891C>T , CM000670.1:g.72156891C>T | GRCh37 |
| NC_000008.9:g.72319445C>T | NCBI36 |
| NG_011735.2:g.122577G>A | |
| NG_011735.3:g.308475G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000340726.8:c.1087G>A MANE Select | ENSP00000342626.3:p.Glu363Lys | |
| ENST00000388741.7:c.985G>A | ENSP00000373393.2:p.Glu329Lys | |
| ENST00000419131.6:c.1035+25084G>A | ENSP00000410176.1:n.1035+25084G>A | |
| ENST00000465115.6:c.*366G>A | ENSP00000428391.1:n.*366G>A | |
| ENST00000493349.2:c.323G>A | ||
| ENST00000496494.6:n.1550G>A | ||
| ENST00000642391.1:c.*817+25084G>A | ENSP00000496700.1:n.*817+25084G>A | |
| ENST00000643681.1:c.1174G>A | ENSP00000495390.1:p.Glu392Lys | |
| ENST00000644229.1:c.1122+25084G>A | ENSP00000494568.1:n.1122+25084G>A | |
| ENST00000644424.1:n.157G>A | ||
| ENST00000644712.1:c.1119+25084G>A | ENSP00000496188.1:n.1119+25084G>A | |
| ENST00000645793.1:c.1087G>A | ENSP00000496255.1:p.Glu363Lys | |
| ENST00000647540.1:c.1087G>A | ENSP00000494438.1:p.Glu363Lys | |
| ENST00000303824.11:c.1069G>A | ENSP00000303221.7:p.Glu357Lys | |
| ENST00000340726.7:c.1087G>A | ENSP00000342626.3:p.Glu363Lys | |
| ENST00000388740.4:c.988G>A | ENSP00000373392.3:p.Glu330Lys | |
| ENST00000388741.6:c.985G>A | ENSP00000373393.2:p.Glu329Lys | |
| ENST00000388742.8:c.1087G>A | ENSP00000373394.4:p.Glu363Lys | |
| ENST00000388743.6:c.1084G>A | ENSP00000373395.2:p.Glu362Lys | |
| ENST00000419131.5:c.1035+25084G>A | ENSP00000410176.1:n.1035+25084G>A | |
| ENST00000465115.5:c.*366G>A | ENSP00000428391.1:n.*366G>A | |
| ENST00000493349.1:c.4G>A | ENSP00000428517.1:p.Glu2Lys | |
| ENST00000496494.5:n.1582G>A | ||
| NM_000503.5:c.1087G>A | NP_000494.2:p.Glu363Lys | |
| NM_001288574.1:c.1069G>A | NP_001275503.1:p.Glu357Lys | |
| NM_001288575.1:c.721G>A | NP_001275504.1:p.Glu241Lys | |
| NM_172058.3:c.1087G>A | NP_742055.1:p.Glu363Lys | |
| NM_172059.3:c.1035+25084G>A | NP_742056.1:n.1035+25084G>A | |
| NM_172060.3:c.988G>A | NP_742057.1:p.Glu330Lys | |
| XM_011517481.1:c.1159G>A | XP_011515783.1:p.Glu387Lys | |
| XM_011517482.1:c.1174G>A | XP_011515784.1:p.Glu392Lys | |
| XM_011517483.1:c.1084G>A | XP_011515785.1:p.Glu362Lys | |
| XM_011517484.1:c.1072G>A | XP_011515786.1:p.Glu358Lys | |
| XM_011517485.1:c.1087G>A | XP_011515787.1:p.Glu363Lys | |
| XM_011517486.1:c.1087G>A | XP_011515788.1:p.Glu363Lys | |
| XM_011517487.1:c.1087G>A | XP_011515789.1:p.Glu363Lys | |
| XM_011517488.1:c.1084G>A | XP_011515790.1:p.Glu362Lys | |
| XM_011517489.1:c.1024G>A | XP_011515791.1:p.Glu342Lys | |
| XM_011517490.1:c.988G>A | XP_011515792.1:p.Glu330Lys | |
| XM_011517491.1:c.988G>A | XP_011515793.1:p.Glu330Lys | |
| XM_011517492.1:c.736G>A | XP_011515794.1:p.Glu246Lys | |
| NM_172059.4:c.1122+25084G>A | NP_742056.2:n.1122+25084G>A | |
| XM_011517483.2:c.1084G>A | XP_011515785.1:p.Glu362Lys | |
| XM_011517484.3:c.1159G>A | XP_011515786.2:p.Glu387Lys | |
| XM_017013201.1:c.1174G>A | XP_016868690.1:p.Glu392Lys | |
| XM_017013202.1:c.1174G>A | XP_016868691.1:p.Glu392Lys | |
| XM_017013203.2:c.1171G>A | XP_016868692.1:p.Glu391Lys | |
| XM_017013204.2:c.1156G>A | XP_016868693.1:p.Glu386Lys | |
| XM_017013205.2:c.1174G>A | XP_016868694.1:p.Glu392Lys | |
| XM_017013206.1:c.1087G>A | XP_016868695.1:p.Glu363Lys | |
| XM_017013207.2:c.1137+25084G>A | XP_016868696.1:n.1137+25084G>A | |
| XM_017013208.2:c.1084G>A | XP_016868697.1:p.Glu362Lys | |
| XM_017013210.2:c.1119+25084G>A | XP_016868699.1:n.1119+25084G>A | |
| XM_017013211.2:c.1024G>A | XP_016868700.1:p.Glu342Lys | |
| XM_017013212.2:c.988G>A | XP_016868701.1:p.Glu330Lys | |
| XM_017013213.1:c.736G>A | XP_016868702.1:p.Glu246Lys | |
| NM_000503.6:c.1087G>A MANE Select | NP_000494.2:p.Glu363Lys | |
| NM_001288574.2:c.1069G>A | NP_001275503.1:p.Glu357Lys | |
| NM_001288575.2:c.721G>A | NP_001275504.1:p.Glu241Lys | |
| NM_001370333.1:c.1174G>A | NP_001357262.1:p.Glu392Lys | |
| NM_001370334.1:c.1087G>A | NP_001357263.1:p.Glu363Lys | |
| NM_001370335.1:c.1087G>A | NP_001357264.1:p.Glu363Lys | |
| NM_001370336.1:c.1119+25084G>A | NP_001357265.1:n.1119+25084G>A | |
| NM_172058.4:c.1087G>A | NP_742055.1:p.Glu363Lys | |
| NM_172059.5:c.1122+25084G>A | NP_742056.2:n.1122+25084G>A |