Canonical Allele Identifier: CA4057232
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 282775
dbSNP Id: rs149901087

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152369064G>C , CM000668.2:g.152369064G>C GRCh38
NC_000006.11:g.152690199G>C , CM000668.1:g.152690199G>C GRCh37
NC_000006.10:g.152731892G>C NCBI36
NG_012855.1:g.273336C>G
NG_012855.2:g.273336C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367255.10:c.9715C>G MANE Select ENSP00000356224.5:p.Gln3239Glu
ENST00000423061.6:c.9736C>G ENSP00000396024.1:p.Gln3246Glu
ENST00000341594.9:c.9781C>G ENSP00000341887.6:p.Gln3261Glu
ENST00000367255.9:c.9715C>G ENSP00000356224.5:p.Gln3239Glu
ENST00000423061.5:c.9736C>G ENSP00000396024.1:p.Gln3246Glu
ENST00000454018.6:n.1063C>G ENSP00000390858.3:p.Gln355Glu
ENST00000469439.1:n.244+407C>G
ENST00000471834.1:n.1264C>G
NM_033071.3:c.9736C>G NP_149062.1:p.Gln3246Glu
NM_182961.3:c.9715C>G NP_892006.3:p.Gln3239Glu
XM_006715407.1:c.9736C>G XP_006715470.1:p.Gln3246Glu
XM_006715408.1:c.9736C>G XP_006715471.1:p.Gln3246Glu
XM_006715409.1:c.9715C>G XP_006715472.1:p.Gln3239Glu
XM_006715410.1:c.9736C>G XP_006715473.1:p.Gln3246Glu
XM_006715411.1:c.9685C>G XP_006715474.1:p.Gln3229Glu
XM_006715412.1:c.9736C>G XP_006715475.1:p.Gln3246Glu
XM_006715413.1:c.9736C>G XP_006715476.1:p.Gln3246Glu
XM_006715414.1:c.9664C>G XP_006715477.1:p.Gln3222Glu
XM_006715415.1:c.9736C>G XP_006715478.1:p.Gln3246Glu
XM_006715416.1:c.9736C>G XP_006715479.1:p.Gln3246Glu
XM_006715417.1:c.9736C>G XP_006715480.1:p.Gln3246Glu
XM_006715420.1:c.9736C>G XP_006715483.1:p.Gln3246Glu
XM_006715421.1:c.9672+407C>G XP_006715484.1:p.=
XM_006715422.1:c.9577C>G XP_006715485.1:p.Gln3193Glu
XM_006715423.1:c.9736C>G XP_006715486.1:p.Gln3246Glu
XM_006715424.1:c.9736C>G XP_006715487.1:p.Gln3246Glu
XM_006715425.1:c.9736C>G XP_006715488.1:p.Gln3246Glu
XM_011535641.1:c.9736C>G XP_011533943.1:p.Gln3246Glu
XM_011535642.1:c.9736C>G XP_011533944.1:p.Gln3246Glu
XM_011535643.1:c.9571C>G XP_011533945.1:p.Gln3191Glu
XM_011535644.1:c.8011C>G XP_011533946.1:p.Gln2671Glu
XM_011535645.1:c.7504C>G XP_011533947.1:p.Gln2502Glu
XM_011535646.1:c.9736C>G XP_011533948.1:p.Gln3246Glu
XM_011535647.1:n.2971C>G XP_011533949.1:p.Gln991Glu
XM_006715408.2:c.9736C>G XP_006715471.1:p.Gln3246Glu
XM_006715410.2:c.9736C>G XP_006715473.1:p.Gln3246Glu
XM_006715412.2:c.9736C>G XP_006715475.1:p.Gln3246Glu
XM_006715413.2:c.9736C>G XP_006715476.1:p.Gln3246Glu
XM_006715415.2:c.9736C>G XP_006715478.1:p.Gln3246Glu
XM_006715416.2:c.9736C>G XP_006715479.1:p.Gln3246Glu
XM_006715417.2:c.9736C>G XP_006715480.1:p.Gln3246Glu
XM_006715420.2:c.9736C>G XP_006715483.1:p.Gln3246Glu
XM_006715421.2:c.9672+407C>G XP_006715484.1:p.=
XM_006715423.2:c.9736C>G XP_006715486.1:p.Gln3246Glu
XM_006715424.2:c.9736C>G XP_006715487.1:p.Gln3246Glu
XM_006715425.2:c.9736C>G XP_006715488.1:p.Gln3246Glu
XM_011535641.2:c.9736C>G XP_011533943.1:p.Gln3246Glu
XM_011535642.2:c.9736C>G XP_011533944.1:p.Gln3246Glu
XM_011535645.2:c.7504C>G XP_011533947.1:p.Gln2502Glu
XM_017010608.1:c.9736C>G XP_016866097.1:p.Gln3246Glu
XM_017010609.1:c.9736C>G XP_016866098.1:p.Gln3246Glu
XM_017010610.1:c.9715C>G XP_016866099.1:p.Gln3239Glu
XM_017010611.2:c.9709C>G XP_016866100.1:p.Gln3237Glu
XM_017010612.1:c.9658C>G XP_016866101.1:p.Gln3220Glu
XM_017010613.1:c.9736C>G XP_016866102.1:p.Gln3246Glu
XM_017010614.1:c.9736C>G XP_016866103.1:p.Gln3246Glu
XM_017010615.1:c.9736C>G XP_016866104.1:p.Gln3246Glu
XM_017010616.1:c.9736C>G XP_016866105.1:p.Gln3246Glu
XM_017010617.1:c.9736C>G XP_016866106.1:p.Gln3246Glu
XM_017010618.1:c.9736C>G XP_016866107.1:p.Gln3246Glu
XM_017010619.1:c.8011C>G XP_016866108.1:p.Gln2671Glu
XR_001743287.1:n.10219C>G
NM_182961.4:c.9715C>G MANE Select NP_892006.3:p.Gln3239Glu
NM_033071.5:c.9736C>G NP_149062.2:p.Gln3246Glu