Canonical Allele Identifier: CA4052909
Gene: SYNE1 HGNC NCBI

Linked Data

dbSNP Id: rs776109498

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152141278C>T , CM000668.2:g.152141278C>T GRCh38
NC_000006.11:g.152462413C>T , CM000668.1:g.152462413C>T GRCh37
NC_000006.10:g.152504106C>T NCBI36
NG_012855.1:g.501122G>A
NG_012855.2:g.501122G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1705G>A MANE Plus Clinical ENSP00000346701.4:p.Glu569Lys
ENST00000367255.10:c.25171G>A MANE Select ENSP00000356224.5:p.Glu8391Lys
ENST00000423061.6:c.25027G>A ENSP00000396024.1:p.Glu8343Lys
ENST00000672154.1:c.573G>A
ENST00000672169.1:c.906G>A
ENST00000673173.1:c.891-1117G>A
ENST00000673451.1:c.943G>A ENSP00000500189.1:p.Glu315Lys
ENST00000341594.9:c.23956G>A ENSP00000341887.6:p.Glu7986Lys
ENST00000347037.9:n.1919G>A
ENST00000354674.4:c.1705G>A ENSP00000346701.4:p.Glu569Lys
ENST00000367251.7:c.4006G>A ENSP00000356220.3:p.Glu1336Lys
ENST00000367255.9:c.25171G>A ENSP00000356224.5:p.Glu8391Lys
ENST00000367256.9:n.8863G>A
ENST00000367257.8:c.3109G>A ENSP00000356226.4:p.Glu1037Lys
ENST00000409694.6:n.8755G>A
ENST00000423061.5:c.25027G>A ENSP00000396024.1:p.Glu8343Lys
ENST00000460912.6:n.1785G>A
ENST00000478916.5:n.4193G>A
ENST00000536990.5:n.2008G>A
ENST00000539504.5:c.1636G>A ENSP00000441052.1:p.Glu546Lys
NM_033071.3:c.25027G>A NP_149062.1:p.Glu8343Lys
NM_182961.3:c.25171G>A NP_892006.3:p.Glu8391Lys
XM_006715407.1:c.25276G>A XP_006715470.1:p.Glu8426Lys
XM_006715408.1:c.25264G>A XP_006715471.1:p.Glu8422Lys
XM_006715409.1:c.25255G>A XP_006715472.1:p.Glu8419Lys
XM_006715410.1:c.25276G>A XP_006715473.1:p.Glu8426Lys
XM_006715411.1:c.25225G>A XP_006715474.1:p.Glu8409Lys
XM_006715412.1:c.25261G>A XP_006715475.1:p.Glu8421Lys
XM_006715413.1:c.25207G>A XP_006715476.1:p.Glu8403Lys
XM_006715414.1:c.25204G>A XP_006715477.1:p.Glu8402Lys
XM_006715415.1:c.25207G>A XP_006715478.1:p.Glu8403Lys
XM_006715416.1:c.25192G>A XP_006715479.1:p.Glu8398Lys
XM_006715417.1:c.25135G>A XP_006715480.1:p.Glu8379Lys
XM_006715420.1:c.25123G>A XP_006715483.1:p.Glu8375Lys
XM_006715421.1:c.25120G>A XP_006715484.1:p.Glu8374Lys
XM_006715422.1:c.25117G>A XP_006715485.1:p.Glu8373Lys
XM_006715423.1:c.25276G>A XP_006715486.1:p.Glu8426Lys
XM_006715424.1:c.25276G>A XP_006715487.1:p.Glu8426Lys
XM_006715425.1:c.25207G>A XP_006715488.1:p.Glu8403Lys
XM_011535641.1:c.25273G>A XP_011533943.1:p.Glu8425Lys
XM_011535642.1:c.25261G>A XP_011533944.1:p.Glu8421Lys
XM_011535643.1:c.25111G>A XP_011533945.1:p.Glu8371Lys
XM_011535644.1:c.23551G>A XP_011533946.1:p.Glu7851Lys
XM_011535645.1:c.23044G>A XP_011533947.1:p.Glu7682Lys
XM_011535647.1:c.18511G>A XP_011533949.1:p.Glu6171Lys
NM_001347701.1:c.1777G>A NP_001334630.1:p.Glu593Lys
NM_001347702.1:c.1705G>A NP_001334631.1:p.Glu569Lys
XM_006715408.2:c.25264G>A XP_006715471.1:p.Glu8422Lys
XM_006715410.2:c.25276G>A XP_006715473.1:p.Glu8426Lys
XM_006715412.2:c.25261G>A XP_006715475.1:p.Glu8421Lys
XM_006715413.2:c.25207G>A XP_006715476.1:p.Glu8403Lys
XM_006715415.2:c.25207G>A XP_006715478.1:p.Glu8403Lys
XM_006715416.2:c.25192G>A XP_006715479.1:p.Glu8398Lys
XM_006715417.2:c.25135G>A XP_006715480.1:p.Glu8379Lys
XM_006715420.2:c.25123G>A XP_006715483.1:p.Glu8375Lys
XM_006715421.2:c.25120G>A XP_006715484.1:p.Glu8374Lys
XM_006715423.2:c.25276G>A XP_006715486.1:p.Glu8426Lys
XM_006715424.2:c.25276G>A XP_006715487.1:p.Glu8426Lys
XM_006715425.2:c.25207G>A XP_006715488.1:p.Glu8403Lys
XM_011535641.2:c.25273G>A XP_011533943.1:p.Glu8425Lys
XM_011535642.2:c.25261G>A XP_011533944.1:p.Glu8421Lys
XM_011535645.2:c.23044G>A XP_011533947.1:p.Glu7682Lys
XM_017010608.1:c.25276G>A XP_016866097.1:p.Glu8426Lys
XM_017010609.1:c.25276G>A XP_016866098.1:p.Glu8426Lys
XM_017010610.1:c.25255G>A XP_016866099.1:p.Glu8419Lys
XM_017010611.2:c.25249G>A XP_016866100.1:p.Glu8417Lys
XM_017010612.1:c.25198G>A XP_016866101.1:p.Glu8400Lys
XM_017010613.1:c.25204G>A XP_016866102.1:p.Glu8402Lys
XM_017010614.1:c.25120G>A XP_016866103.1:p.Glu8374Lys
XM_017010615.1:c.25051G>A XP_016866104.1:p.Glu8351Lys
XM_017010616.1:c.25207G>A XP_016866105.1:p.Glu8403Lys
XM_017010617.1:c.25204G>A XP_016866106.1:p.Glu8402Lys
XM_017010618.1:c.25192G>A XP_016866107.1:p.Glu8398Lys
XM_017010619.1:c.23551G>A XP_016866108.1:p.Glu7851Lys
NM_182961.4:c.25171G>A MANE Select NP_892006.3:p.Glu8391Lys
NM_001347701.2:c.1777G>A NP_001334630.1:p.Glu593Lys
NM_001347702.2:c.1705G>A MANE Plus Clinical NP_001334631.1:p.Glu569Lys
NM_033071.5:c.25027G>A NP_149062.2:p.Glu8343Lys