Linked Data
ClinVar Variation Id:
499024
dbSNP Id:
rs550697327
ExAC:
6:152443620 C / T
gnomAD v2:
6-152443620-C-T
gnomAD v3:
6-152122485-C-T
gnomAD v4:
6-152122485-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152122485C>T , CM000668.2:g.152122485C>T | GRCh38 |
| NC_000006.11:g.152443620C>T , CM000668.1:g.152443620C>T | GRCh37 |
| NC_000006.10:g.152485313C>T | NCBI36 |
| NG_012855.1:g.519915G>A | |
| NG_008493.2:g.470795C>T | |
| NG_012855.2:g.519915G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.2879G>A (SYNE1) MANE Plus Clinical | ENSP00000346701.4:p.Arg960Gln | |
| ENST00000367255.10:c.26345G>A (SYNE1) MANE Select | ENSP00000356224.5:p.Arg8782Gln | |
| ENST00000423061.6:c.26201G>A (SYNE1) | ENSP00000396024.1:p.Arg8734Gln | |
| ENST00000672154.1:c.1688G>A (SYNE1) | ||
| ENST00000672169.1:c.2063G>A (SYNE1) | ||
| ENST00000673173.1:c.1930G>A (SYNE1) | ||
| ENST00000673451.1:c.2195G>A (SYNE1) | ENSP00000500189.1:n.2195G>A | |
| ENST00000341594.9:c.25130G>A (SYNE1) | ENSP00000341887.6:p.Arg8377Gln | |
| ENST00000347037.9:n.3093G>A (SYNE1) | ||
| ENST00000354674.4:c.2879G>A (SYNE1) | ENSP00000346701.4:p.Arg960Gln | |
| ENST00000367251.7:c.5121G>A (SYNE1) | ENSP00000356220.3:n.5121G>A | |
| ENST00000367255.9:c.26345G>A (SYNE1) | ENSP00000356224.5:p.Arg8782Gln | |
| ENST00000367256.9:n.10037G>A (SYNE1) | ||
| ENST00000367257.8:c.4224G>A (SYNE1) | ENSP00000356226.4:n.4224G>A | |
| ENST00000409694.6:n.9929G>A (SYNE1) | ||
| ENST00000423061.5:c.26201G>A (SYNE1) | ENSP00000396024.1:p.Arg8734Gln | |
| ENST00000427531.6:c.851-2781C>T (ESR1) | ENSP00000394721.2:n.851-2781C>T | |
| ENST00000460912.6:n.2959G>A (SYNE1) | ||
| ENST00000478916.5:n.6982G>A (SYNE1) | ||
| ENST00000539504.5:c.2810G>A (SYNE1) | ENSP00000441052.1:p.Arg937Gln | |
| NM_033071.3:c.26201G>A (SYNE1) | NP_149062.1:p.Arg8734Gln | |
| NM_182961.3:c.26345G>A (SYNE1) | NP_892006.3:p.Arg8782Gln | |
| XM_006715407.1:c.26492G>A (SYNE1) | XP_006715470.1:p.Arg8831Gln | |
| XM_006715408.1:c.26480G>A (SYNE1) | XP_006715471.1:p.Arg8827Gln | |
| XM_006715409.1:c.26471G>A (SYNE1) | XP_006715472.1:p.Arg8824Gln | |
| XM_006715410.1:c.26450G>A (SYNE1) | XP_006715473.1:p.Arg8817Gln | |
| XM_006715411.1:c.26441G>A (SYNE1) | XP_006715474.1:p.Arg8814Gln | |
| XM_006715412.1:c.26435G>A (SYNE1) | XP_006715475.1:p.Arg8812Gln | |
| XM_006715413.1:c.26423G>A (SYNE1) | XP_006715476.1:p.Arg8808Gln | |
| XM_006715414.1:c.26420G>A (SYNE1) | XP_006715477.1:p.Arg8807Gln | |
| XM_006715415.1:c.26381G>A (SYNE1) | XP_006715478.1:p.Arg8794Gln | |
| XM_006715416.1:c.26366G>A (SYNE1) | XP_006715479.1:p.Arg8789Gln | |
| XM_006715417.1:c.26351G>A (SYNE1) | XP_006715480.1:p.Arg8784Gln | |
| XM_006715420.1:c.26339G>A (SYNE1) | XP_006715483.1:p.Arg8780Gln | |
| XM_006715421.1:c.26336G>A (SYNE1) | XP_006715484.1:p.Arg8779Gln | |
| XM_006715422.1:c.26333G>A (SYNE1) | XP_006715485.1:p.Arg8778Gln | |
| XM_006715423.1:c.*156G>A (SYNE1) | XP_006715486.1:n.*156G>A | |
| XM_006715424.1:c.*156G>A (SYNE1) | XP_006715487.1:n.*156G>A | |
| XM_006715425.1:c.*156G>A (SYNE1) | XP_006715488.1:n.*156G>A | |
| XM_011535641.1:c.26489G>A (SYNE1) | XP_011533943.1:p.Arg8830Gln | |
| XM_011535642.1:c.26477G>A (SYNE1) | XP_011533944.1:p.Arg8826Gln | |
| XM_011535643.1:c.26327G>A (SYNE1) | XP_011533945.1:p.Arg8776Gln | |
| XM_011535644.1:c.24767G>A (SYNE1) | XP_011533946.1:p.Arg8256Gln | |
| XM_011535645.1:c.24260G>A (SYNE1) | XP_011533947.1:p.Arg8087Gln | |
| XM_011535647.1:c.19727G>A (SYNE1) | XP_011533949.1:p.Arg6576Gln | |
| NM_001328100.1:c.851-2781C>T (ESR1) | NP_001315029.1:n.851-2781C>T | |
| NM_001347701.1:c.*156G>A (SYNE1) | NP_001334630.1:n.*156G>A | |
| NM_001347702.1:c.2879G>A (SYNE1) | NP_001334631.1:p.Arg960Gln | |
| XM_006715408.2:c.26480G>A (SYNE1) | XP_006715471.1:p.Arg8827Gln | |
| XM_006715410.2:c.26450G>A (SYNE1) | XP_006715473.1:p.Arg8817Gln | |
| XM_006715412.2:c.26435G>A (SYNE1) | XP_006715475.1:p.Arg8812Gln | |
| XM_006715413.2:c.26423G>A (SYNE1) | XP_006715476.1:p.Arg8808Gln | |
| XM_006715415.2:c.26381G>A (SYNE1) | XP_006715478.1:p.Arg8794Gln | |
| XM_006715416.2:c.26366G>A (SYNE1) | XP_006715479.1:p.Arg8789Gln | |
| XM_006715417.2:c.26351G>A (SYNE1) | XP_006715480.1:p.Arg8784Gln | |
| XM_006715420.2:c.26339G>A (SYNE1) | XP_006715483.1:p.Arg8780Gln | |
| XM_006715421.2:c.26336G>A (SYNE1) | XP_006715484.1:p.Arg8779Gln | |
| XM_006715423.2:c.*156G>A (SYNE1) | XP_006715486.1:n.*156G>A | |
| XM_006715424.2:c.*156G>A (SYNE1) | XP_006715487.1:n.*156G>A | |
| XM_006715425.2:c.*156G>A (SYNE1) | XP_006715488.1:n.*156G>A | |
| XM_011535641.2:c.26489G>A (SYNE1) | XP_011533943.1:p.Arg8830Gln | |
| XM_011535642.2:c.26477G>A (SYNE1) | XP_011533944.1:p.Arg8826Gln | |
| XM_011535645.2:c.24260G>A (SYNE1) | XP_011533947.1:p.Arg8087Gln | |
| XM_017010608.1:c.26492G>A (SYNE1) | XP_016866097.1:p.Arg8831Gln | |
| XM_017010609.1:c.26492G>A (SYNE1) | XP_016866098.1:p.Arg8831Gln | |
| XM_017010610.1:c.26471G>A (SYNE1) | XP_016866099.1:p.Arg8824Gln | |
| XM_017010611.2:c.26465G>A (SYNE1) | XP_016866100.1:p.Arg8822Gln | |
| XM_017010612.1:c.26414G>A (SYNE1) | XP_016866101.1:p.Arg8805Gln | |
| XM_017010613.1:c.26378G>A (SYNE1) | XP_016866102.1:p.Arg8793Gln | |
| XM_017010614.1:c.26336G>A (SYNE1) | XP_016866103.1:p.Arg8779Gln | |
| XM_017010615.1:c.26225G>A (SYNE1) | XP_016866104.1:p.Arg8742Gln | |
| XM_017010616.1:c.*156G>A (SYNE1) | XP_016866105.1:n.*156G>A | |
| XM_017010617.1:c.*156G>A (SYNE1) | XP_016866106.1:n.*156G>A | |
| XM_017010618.1:c.*156G>A (SYNE1) | XP_016866107.1:n.*156G>A | |
| XM_017010619.1:c.24767G>A (SYNE1) | XP_016866108.1:p.Arg8256Gln | |
| NM_182961.4:c.26345G>A (SYNE1) MANE Select | NP_892006.3:p.Arg8782Gln | |
| NM_001328100.2:c.851-2781C>T (ESR1) | NP_001315029.1:n.851-2781C>T | |
| NM_001347701.2:c.*156G>A (SYNE1) | NP_001334630.1:n.*156G>A | |
| NM_001347702.2:c.2879G>A (SYNE1) MANE Plus Clinical | NP_001334631.1:p.Arg960Gln | |
| NM_033071.5:c.26201G>A (SYNE1) | NP_149062.2:p.Arg8734Gln |