Canonical Allele Identifier: CA150165450
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 586730
dbSNP Id: rs754577367

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152139973C>T , CM000668.2:g.152139973C>T GRCh38
NC_000006.11:g.152461108C>T , CM000668.1:g.152461108C>T GRCh37
NC_000006.10:g.152502801C>T NCBI36
NG_012855.1:g.502427G>A
NG_012855.2:g.502427G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1969G>A MANE Plus Clinical ENSP00000346701.4:p.Glu657Lys
ENST00000367255.10:c.25435G>A MANE Select ENSP00000356224.5:p.Glu8479Lys
ENST00000423061.6:c.25291G>A ENSP00000396024.1:p.Glu8431Lys
ENST00000672154.1:c.837G>A
ENST00000672169.1:c.1170G>A
ENST00000673173.1:c.1079G>A
ENST00000673451.1:c.1207G>A ENSP00000500189.1:p.Glu403Lys
ENST00000341594.9:c.24220G>A ENSP00000341887.6:p.Glu8074Lys
ENST00000347037.9:n.2183G>A
ENST00000354674.4:c.1969G>A ENSP00000346701.4:p.Glu657Lys
ENST00000367251.7:c.4270G>A ENSP00000356220.3:p.Glu1424Lys
ENST00000367255.9:c.25435G>A ENSP00000356224.5:p.Glu8479Lys
ENST00000367256.9:n.9127G>A
ENST00000367257.8:c.3373G>A ENSP00000356226.4:p.Glu1125Lys
ENST00000409694.6:n.9019G>A
ENST00000423061.5:c.25291G>A ENSP00000396024.1:p.Glu8431Lys
ENST00000460912.6:n.2049G>A
ENST00000478916.5:n.4457G>A
ENST00000536990.5:n.2272G>A
ENST00000539504.5:c.1900G>A ENSP00000441052.1:p.Glu634Lys
NM_033071.3:c.25291G>A NP_149062.1:p.Glu8431Lys
NM_182961.3:c.25435G>A NP_892006.3:p.Glu8479Lys
XM_006715407.1:c.25540G>A XP_006715470.1:p.Glu8514Lys
XM_006715408.1:c.25528G>A XP_006715471.1:p.Glu8510Lys
XM_006715409.1:c.25519G>A XP_006715472.1:p.Glu8507Lys
XM_006715410.1:c.25540G>A XP_006715473.1:p.Glu8514Lys
XM_006715411.1:c.25489G>A XP_006715474.1:p.Glu8497Lys
XM_006715412.1:c.25525G>A XP_006715475.1:p.Glu8509Lys
XM_006715413.1:c.25471G>A XP_006715476.1:p.Glu8491Lys
XM_006715414.1:c.25468G>A XP_006715477.1:p.Glu8490Lys
XM_006715415.1:c.25471G>A XP_006715478.1:p.Glu8491Lys
XM_006715416.1:c.25456G>A XP_006715479.1:p.Glu8486Lys
XM_006715417.1:c.25399G>A XP_006715480.1:p.Glu8467Lys
XM_006715420.1:c.25387G>A XP_006715483.1:p.Glu8463Lys
XM_006715421.1:c.25384G>A XP_006715484.1:p.Glu8462Lys
XM_006715422.1:c.25381G>A XP_006715485.1:p.Glu8461Lys
XM_006715423.1:c.25540G>A XP_006715486.1:p.Glu8514Lys
XM_006715424.1:c.25540G>A XP_006715487.1:p.Glu8514Lys
XM_006715425.1:c.25471G>A XP_006715488.1:p.Glu8491Lys
XM_011535641.1:c.25537G>A XP_011533943.1:p.Glu8513Lys
XM_011535642.1:c.25525G>A XP_011533944.1:p.Glu8509Lys
XM_011535643.1:c.25375G>A XP_011533945.1:p.Glu8459Lys
XM_011535644.1:c.23815G>A XP_011533946.1:p.Glu7939Lys
XM_011535645.1:c.23308G>A XP_011533947.1:p.Glu7770Lys
XM_011535647.1:c.18775G>A XP_011533949.1:p.Glu6259Lys
NM_001347701.1:c.2041G>A NP_001334630.1:p.Glu681Lys
NM_001347702.1:c.1969G>A NP_001334631.1:p.Glu657Lys
XM_006715408.2:c.25528G>A XP_006715471.1:p.Glu8510Lys
XM_006715410.2:c.25540G>A XP_006715473.1:p.Glu8514Lys
XM_006715412.2:c.25525G>A XP_006715475.1:p.Glu8509Lys
XM_006715413.2:c.25471G>A XP_006715476.1:p.Glu8491Lys
XM_006715415.2:c.25471G>A XP_006715478.1:p.Glu8491Lys
XM_006715416.2:c.25456G>A XP_006715479.1:p.Glu8486Lys
XM_006715417.2:c.25399G>A XP_006715480.1:p.Glu8467Lys
XM_006715420.2:c.25387G>A XP_006715483.1:p.Glu8463Lys
XM_006715421.2:c.25384G>A XP_006715484.1:p.Glu8462Lys
XM_006715423.2:c.25540G>A XP_006715486.1:p.Glu8514Lys
XM_006715424.2:c.25540G>A XP_006715487.1:p.Glu8514Lys
XM_006715425.2:c.25471G>A XP_006715488.1:p.Glu8491Lys
XM_011535641.2:c.25537G>A XP_011533943.1:p.Glu8513Lys
XM_011535642.2:c.25525G>A XP_011533944.1:p.Glu8509Lys
XM_011535645.2:c.23308G>A XP_011533947.1:p.Glu7770Lys
XM_017010608.1:c.25540G>A XP_016866097.1:p.Glu8514Lys
XM_017010609.1:c.25540G>A XP_016866098.1:p.Glu8514Lys
XM_017010610.1:c.25519G>A XP_016866099.1:p.Glu8507Lys
XM_017010611.2:c.25513G>A XP_016866100.1:p.Glu8505Lys
XM_017010612.1:c.25462G>A XP_016866101.1:p.Glu8488Lys
XM_017010613.1:c.25468G>A XP_016866102.1:p.Glu8490Lys
XM_017010614.1:c.25384G>A XP_016866103.1:p.Glu8462Lys
XM_017010615.1:c.25315G>A XP_016866104.1:p.Glu8439Lys
XM_017010616.1:c.25471G>A XP_016866105.1:p.Glu8491Lys
XM_017010617.1:c.25468G>A XP_016866106.1:p.Glu8490Lys
XM_017010618.1:c.25456G>A XP_016866107.1:p.Glu8486Lys
XM_017010619.1:c.23815G>A XP_016866108.1:p.Glu7939Lys
NM_182961.4:c.25435G>A MANE Select NP_892006.3:p.Glu8479Lys
NM_001347701.2:c.2041G>A NP_001334630.1:p.Glu681Lys
NM_001347702.2:c.1969G>A MANE Plus Clinical NP_001334631.1:p.Glu657Lys
NM_033071.5:c.25291G>A NP_149062.2:p.Glu8431Lys