Canonical Allele Identifier: CA366086843
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152151969C>G , CM000668.2:g.152151969C>G GRCh38
NC_000006.11:g.152473104C>G , CM000668.1:g.152473104C>G GRCh37
NC_000006.10:g.152514797C>G NCBI36
NG_012855.1:g.490431G>C
NG_012855.2:g.490431G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.767G>C MANE Plus Clinical ENSP00000346701.4:p.Arg256Pro
ENST00000367255.10:c.24302G>C MANE Select ENSP00000356224.5:p.Arg8101Pro
ENST00000423061.6:c.24089G>C ENSP00000396024.1:p.Arg8030Pro
ENST00000672169.1:c.37G>C
ENST00000673173.1:c.216G>C
ENST00000673451.1:c.74G>C ENSP00000500189.1:p.Arg25Pro
ENST00000341594.9:c.23087G>C ENSP00000341887.6:p.Arg7696Pro
ENST00000347037.9:n.981G>C
ENST00000354674.4:c.767G>C ENSP00000346701.4:p.Arg256Pro
ENST00000367251.7:c.3068G>C ENSP00000356220.3:p.Arg1023Pro
ENST00000367255.9:c.24302G>C ENSP00000356224.5:p.Arg8101Pro
ENST00000367256.9:n.7994G>C
ENST00000367257.8:c.2240G>C ENSP00000356226.4:p.Arg747Pro
ENST00000409694.6:n.7886G>C
ENST00000423061.5:c.24089G>C ENSP00000396024.1:p.Arg8030Pro
ENST00000460912.6:n.847G>C
ENST00000476519.1:n.364G>C
ENST00000536990.5:n.1139G>C
ENST00000539504.5:c.767G>C ENSP00000441052.1:p.Arg256Pro
NM_033071.3:c.24089G>C NP_149062.1:p.Arg8030Pro
NM_182961.3:c.24302G>C NP_892006.3:p.Arg8101Pro
XM_006715407.1:c.24338G>C XP_006715470.1:p.Arg8113Pro
XM_006715408.1:c.24326G>C XP_006715471.1:p.Arg8109Pro
XM_006715409.1:c.24317G>C XP_006715472.1:p.Arg8106Pro
XM_006715410.1:c.24338G>C XP_006715473.1:p.Arg8113Pro
XM_006715411.1:c.24287G>C XP_006715474.1:p.Arg8096Pro
XM_006715412.1:c.24323G>C XP_006715475.1:p.Arg8108Pro
XM_006715413.1:c.24338G>C XP_006715476.1:p.Arg8113Pro
XM_006715414.1:c.24266G>C XP_006715477.1:p.Arg8089Pro
XM_006715415.1:c.24338G>C XP_006715478.1:p.Arg8113Pro
XM_006715416.1:c.24323G>C XP_006715479.1:p.Arg8108Pro
XM_006715417.1:c.24197G>C XP_006715480.1:p.Arg8066Pro
XM_006715420.1:c.24185G>C XP_006715483.1:p.Arg8062Pro
XM_006715421.1:c.24182G>C XP_006715484.1:p.Arg8061Pro
XM_006715422.1:c.24179G>C XP_006715485.1:p.Arg8060Pro
XM_006715423.1:c.24338G>C XP_006715486.1:p.Arg8113Pro
XM_006715424.1:c.24338G>C XP_006715487.1:p.Arg8113Pro
XM_006715425.1:c.24338G>C XP_006715488.1:p.Arg8113Pro
XM_011535641.1:c.24335G>C XP_011533943.1:p.Arg8112Pro
XM_011535642.1:c.24323G>C XP_011533944.1:p.Arg8108Pro
XM_011535643.1:c.24173G>C XP_011533945.1:p.Arg8058Pro
XM_011535644.1:c.22613G>C XP_011533946.1:p.Arg7538Pro
XM_011535645.1:c.22106G>C XP_011533947.1:p.Arg7369Pro
XM_011535647.1:c.17573G>C XP_011533949.1:p.Arg5858Pro
NM_001347701.1:c.908G>C NP_001334630.1:p.Arg303Pro
NM_001347702.1:c.767G>C NP_001334631.1:p.Arg256Pro
XM_006715408.2:c.24326G>C XP_006715471.1:p.Arg8109Pro
XM_006715410.2:c.24338G>C XP_006715473.1:p.Arg8113Pro
XM_006715412.2:c.24323G>C XP_006715475.1:p.Arg8108Pro
XM_006715413.2:c.24338G>C XP_006715476.1:p.Arg8113Pro
XM_006715415.2:c.24338G>C XP_006715478.1:p.Arg8113Pro
XM_006715416.2:c.24323G>C XP_006715479.1:p.Arg8108Pro
XM_006715417.2:c.24197G>C XP_006715480.1:p.Arg8066Pro
XM_006715420.2:c.24185G>C XP_006715483.1:p.Arg8062Pro
XM_006715421.2:c.24182G>C XP_006715484.1:p.Arg8061Pro
XM_006715423.2:c.24338G>C XP_006715486.1:p.Arg8113Pro
XM_006715424.2:c.24338G>C XP_006715487.1:p.Arg8113Pro
XM_006715425.2:c.24338G>C XP_006715488.1:p.Arg8113Pro
XM_011535641.2:c.24335G>C XP_011533943.1:p.Arg8112Pro
XM_011535642.2:c.24323G>C XP_011533944.1:p.Arg8108Pro
XM_011535645.2:c.22106G>C XP_011533947.1:p.Arg7369Pro
XM_017010608.1:c.24338G>C XP_016866097.1:p.Arg8113Pro
XM_017010609.1:c.24338G>C XP_016866098.1:p.Arg8113Pro
XM_017010610.1:c.24317G>C XP_016866099.1:p.Arg8106Pro
XM_017010611.2:c.24311G>C XP_016866100.1:p.Arg8104Pro
XM_017010612.1:c.24260G>C XP_016866101.1:p.Arg8087Pro
XM_017010613.1:c.24335G>C XP_016866102.1:p.Arg8112Pro
XM_017010614.1:c.24182G>C XP_016866103.1:p.Arg8061Pro
XM_017010615.1:c.24182G>C XP_016866104.1:p.Arg8061Pro
XM_017010616.1:c.24338G>C XP_016866105.1:p.Arg8113Pro
XM_017010617.1:c.24335G>C XP_016866106.1:p.Arg8112Pro
XM_017010618.1:c.24323G>C XP_016866107.1:p.Arg8108Pro
XM_017010619.1:c.22613G>C XP_016866108.1:p.Arg7538Pro
NM_182961.4:c.24302G>C MANE Select NP_892006.3:p.Arg8101Pro
NM_001347701.2:c.908G>C NP_001334630.1:p.Arg303Pro
NM_001347702.2:c.767G>C MANE Plus Clinical NP_001334631.1:p.Arg256Pro
NM_033071.5:c.24089G>C NP_149062.2:p.Arg8030Pro