Canonical Allele Identifier: CA366086882
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152151990T>C , CM000668.2:g.152151990T>C GRCh38
NC_000006.11:g.152473125T>C , CM000668.1:g.152473125T>C GRCh37
NC_000006.10:g.152514818T>C NCBI36
NG_012855.1:g.490410A>G
NG_012855.2:g.490410A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354674.5:c.746A>G MANE Plus Clinical ENSP00000346701.4:p.Lys249Arg
ENST00000367255.10:c.24281A>G MANE Select ENSP00000356224.5:p.Lys8094Arg
ENST00000423061.6:c.24068A>G ENSP00000396024.1:p.Lys8023Arg
ENST00000672169.1:c.16A>G
ENST00000673173.1:c.195A>G
ENST00000673451.1:c.53A>G ENSP00000500189.1:p.Lys18Arg
ENST00000341594.9:c.23066A>G ENSP00000341887.6:p.Lys7689Arg
ENST00000347037.9:n.960A>G
ENST00000354674.4:c.746A>G ENSP00000346701.4:p.Lys249Arg
ENST00000367251.7:c.3047A>G ENSP00000356220.3:p.Lys1016Arg
ENST00000367255.9:c.24281A>G ENSP00000356224.5:p.Lys8094Arg
ENST00000367256.9:n.7973A>G
ENST00000367257.8:c.2219A>G ENSP00000356226.4:p.Lys740Arg
ENST00000409694.6:n.7865A>G
ENST00000423061.5:c.24068A>G ENSP00000396024.1:p.Lys8023Arg
ENST00000460912.6:n.826A>G
ENST00000476519.1:n.343A>G
ENST00000536990.5:n.1118A>G
ENST00000539504.5:c.746A>G ENSP00000441052.1:p.Lys249Arg
NM_033071.3:c.24068A>G NP_149062.1:p.Lys8023Arg
NM_182961.3:c.24281A>G NP_892006.3:p.Lys8094Arg
XM_006715407.1:c.24317A>G XP_006715470.1:p.Lys8106Arg
XM_006715408.1:c.24305A>G XP_006715471.1:p.Lys8102Arg
XM_006715409.1:c.24296A>G XP_006715472.1:p.Lys8099Arg
XM_006715410.1:c.24317A>G XP_006715473.1:p.Lys8106Arg
XM_006715411.1:c.24266A>G XP_006715474.1:p.Lys8089Arg
XM_006715412.1:c.24302A>G XP_006715475.1:p.Lys8101Arg
XM_006715413.1:c.24317A>G XP_006715476.1:p.Lys8106Arg
XM_006715414.1:c.24245A>G XP_006715477.1:p.Lys8082Arg
XM_006715415.1:c.24317A>G XP_006715478.1:p.Lys8106Arg
XM_006715416.1:c.24302A>G XP_006715479.1:p.Lys8101Arg
XM_006715417.1:c.24176A>G XP_006715480.1:p.Lys8059Arg
XM_006715420.1:c.24164A>G XP_006715483.1:p.Lys8055Arg
XM_006715421.1:c.24161A>G XP_006715484.1:p.Lys8054Arg
XM_006715422.1:c.24158A>G XP_006715485.1:p.Lys8053Arg
XM_006715423.1:c.24317A>G XP_006715486.1:p.Lys8106Arg
XM_006715424.1:c.24317A>G XP_006715487.1:p.Lys8106Arg
XM_006715425.1:c.24317A>G XP_006715488.1:p.Lys8106Arg
XM_011535641.1:c.24314A>G XP_011533943.1:p.Lys8105Arg
XM_011535642.1:c.24302A>G XP_011533944.1:p.Lys8101Arg
XM_011535643.1:c.24152A>G XP_011533945.1:p.Lys8051Arg
XM_011535644.1:c.22592A>G XP_011533946.1:p.Lys7531Arg
XM_011535645.1:c.22085A>G XP_011533947.1:p.Lys7362Arg
XM_011535647.1:c.17552A>G XP_011533949.1:p.Lys5851Arg
NM_001347701.1:c.887A>G NP_001334630.1:p.Lys296Arg
NM_001347702.1:c.746A>G NP_001334631.1:p.Lys249Arg
XM_006715408.2:c.24305A>G XP_006715471.1:p.Lys8102Arg
XM_006715410.2:c.24317A>G XP_006715473.1:p.Lys8106Arg
XM_006715412.2:c.24302A>G XP_006715475.1:p.Lys8101Arg
XM_006715413.2:c.24317A>G XP_006715476.1:p.Lys8106Arg
XM_006715415.2:c.24317A>G XP_006715478.1:p.Lys8106Arg
XM_006715416.2:c.24302A>G XP_006715479.1:p.Lys8101Arg
XM_006715417.2:c.24176A>G XP_006715480.1:p.Lys8059Arg
XM_006715420.2:c.24164A>G XP_006715483.1:p.Lys8055Arg
XM_006715421.2:c.24161A>G XP_006715484.1:p.Lys8054Arg
XM_006715423.2:c.24317A>G XP_006715486.1:p.Lys8106Arg
XM_006715424.2:c.24317A>G XP_006715487.1:p.Lys8106Arg
XM_006715425.2:c.24317A>G XP_006715488.1:p.Lys8106Arg
XM_011535641.2:c.24314A>G XP_011533943.1:p.Lys8105Arg
XM_011535642.2:c.24302A>G XP_011533944.1:p.Lys8101Arg
XM_011535645.2:c.22085A>G XP_011533947.1:p.Lys7362Arg
XM_017010608.1:c.24317A>G XP_016866097.1:p.Lys8106Arg
XM_017010609.1:c.24317A>G XP_016866098.1:p.Lys8106Arg
XM_017010610.1:c.24296A>G XP_016866099.1:p.Lys8099Arg
XM_017010611.2:c.24290A>G XP_016866100.1:p.Lys8097Arg
XM_017010612.1:c.24239A>G XP_016866101.1:p.Lys8080Arg
XM_017010613.1:c.24314A>G XP_016866102.1:p.Lys8105Arg
XM_017010614.1:c.24161A>G XP_016866103.1:p.Lys8054Arg
XM_017010615.1:c.24161A>G XP_016866104.1:p.Lys8054Arg
XM_017010616.1:c.24317A>G XP_016866105.1:p.Lys8106Arg
XM_017010617.1:c.24314A>G XP_016866106.1:p.Lys8105Arg
XM_017010618.1:c.24302A>G XP_016866107.1:p.Lys8101Arg
XM_017010619.1:c.22592A>G XP_016866108.1:p.Lys7531Arg
NM_182961.4:c.24281A>G MANE Select NP_892006.3:p.Lys8094Arg
NM_001347701.2:c.887A>G NP_001334630.1:p.Lys296Arg
NM_001347702.2:c.746A>G MANE Plus Clinical NP_001334631.1:p.Lys249Arg
NM_033071.5:c.24068A>G NP_149062.2:p.Lys8023Arg