Linked Data
ClinVar Variation Id:
144006
ClinVar RCV Id:
RCV000133515
RCV000698604
RCV000735313
RCV000735320
RCV001027623
RCV001090648
RCV003156074
dbSNP Id:
rs587777630
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.190986921G>A , CM000664.2:g.190986921G>A | GRCh38 |
| NC_000002.11:g.191851647G>A , CM000664.1:g.191851647G>A | GRCh37 |
| NC_000002.10:g.191559892G>A | NCBI36 |
| NG_008294.1:g.32330C>T , LRG_111:g.32330C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698141.1:c.1154C>T | ENSP00000513582.1:p.Thr385Met | |
| ENST00000698142.1:c.1094C>T | ENSP00000513583.1:p.Thr365Met | |
| ENST00000698143.1:n.1314C>T | ||
| ENST00000698144.1:c.*480C>T | ENSP00000513584.1:n.*480C>T | |
| ENST00000698145.1:c.633+11296C>T | ENSP00000513585.1:n.633+11296C>T | |
| ENST00000698146.1:c.*904C>T | ENSP00000513586.1:n.*904C>T | |
| ENST00000698147.1:n.1481C>T | ||
| ENST00000698148.1:n.1481C>T | ||
| ENST00000698149.1:c.1154C>T | ENSP00000513587.1:p.Thr385Met | |
| ENST00000698151.1:n.1481C>T | ||
| ENST00000361099.8:c.1154C>T MANE Select | ENSP00000354394.4:p.Thr385Met | |
| ENST00000415035.2:c.1154C>T | ENSP00000388240.2:p.Thr385Met | |
| ENST00000423282.2:c.129-9896C>T | ENSP00000388772.2:n.129-9896C>T | |
| ENST00000424722.6:c.1064C>T | ENSP00000402548.2:p.Thr355Met | |
| ENST00000452281.6:c.*480C>T | ENSP00000394512.1:n.*480C>T | |
| ENST00000540176.6:c.1154C>T | ENSP00000438703.2:p.Thr385Met | |
| ENST00000673734.1:c.*321C>T | ENSP00000501040.1:n.*321C>T | |
| ENST00000673777.1:c.1148C>T | ENSP00000500982.1:p.Thr383Met | |
| ENST00000673816.1:c.1154C>T | ENSP00000501127.1:p.Thr385Met | |
| ENST00000673841.1:c.1154C>T | ENSP00000501225.1:p.Thr385Met | |
| ENST00000673847.1:c.1154C>T | ENSP00000501185.1:p.Thr385Met | |
| ENST00000673858.1:c.*480C>T | ENSP00000501196.1:n.*480C>T | |
| ENST00000673859.1:n.1453C>T | ||
| ENST00000673863.1:c.39-3163C>T | ENSP00000501286.1:n.39-3163C>T | |
| ENST00000673885.1:c.1154C>T | ENSP00000501159.1:p.Thr385Met | |
| ENST00000673942.1:c.1148C>T | ENSP00000501145.1:p.Thr383Met | |
| ENST00000673952.1:c.1154C>T | ENSP00000501115.1:p.Thr385Met | |
| ENST00000674028.1:n.311-9880C>T | ||
| ENST00000674080.1:c.1154C>T | ENSP00000501164.1:p.Thr385Met | |
| ENST00000674081.1:c.1154C>T | ENSP00000501289.1:p.Thr385Met | |
| ENST00000674153.1:c.1154C>T | ENSP00000501120.1:p.Thr385Met | |
| ENST00000361099.7:c.1154C>T | ENSP00000354394.3:p.Thr385Met | |
| ENST00000392322.7:c.1154C>T | ENSP00000376136.3:p.Thr385Met | |
| ENST00000392323.6:c.1160C>T | ENSP00000376137.2:p.Thr387Met | |
| ENST00000409465.5:c.1154C>T | ENSP00000386244.1:p.Thr385Met | |
| ENST00000452281.5:c.*480C>T | ENSP00000394512.1:n.*480C>T | |
| ENST00000540176.5:c.*480C>T | ENSP00000438703.1:n.*480C>T | |
| NM_007315.3:c.1154C>T , LRG_111t1:c.1154C>T | NP_009330.1:p.Thr385Met | |
| NM_139266.2:c.1154C>T | NP_644671.1:p.Thr385Met | |
| XM_006712718.1:c.1154C>T | XP_006712781.1:p.Thr385Met | |
| XM_017004783.2:c.1160C>T | XP_016860272.1:p.Thr387Met | |
| XR_001738914.2:n.1547C>T | ||
| XR_001738915.2:n.1489C>T | ||
| NM_007315.4:c.1154C>T MANE Select | NP_009330.1:p.Thr385Met | |
| NM_001384880.1:c.1094C>T | NP_001371809.1:p.Thr365Met | |
| NM_001384881.1:c.1160C>T | NP_001371810.1:p.Thr387Met | |
| NM_001384882.1:c.1148C>T | NP_001371811.1:p.Thr383Met | |
| NM_001384883.1:c.1055C>T | NP_001371812.1:p.Thr352Met | |
| NM_001384884.1:c.1160C>T | NP_001371813.1:p.Thr387Met | |
| NM_001384885.1:c.995C>T | NP_001371814.1:p.Thr332Met | |
| NM_001384886.1:c.1154C>T | NP_001371815.1:p.Thr385Met | |
| NM_001384887.1:c.1061C>T | NP_001371816.1:p.Thr354Met | |
| NM_001384888.1:c.1124C>T | NP_001371817.1:p.Thr375Met | |
| NM_001384889.1:c.1154C>T | NP_001371818.1:p.Thr385Met | |
| NM_001384890.1:c.1064C>T | NP_001371819.1:p.Thr355Met | |
| NM_001384891.1:c.1190C>T | NP_001371820.1:p.Thr397Met | |
| NM_139266.3:c.1154C>T | NP_644671.1:p.Thr385Met |