Canonical Allele Identifier: CA1673209264
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152143647C= , CM000668.2:g.152143647C= GRCh38
NC_000006.11:g.152464782C= , CM000668.1:g.152464782C= GRCh37
NC_000006.10:g.152506475C= NCBI36
NG_012855.1:g.498753G=
NG_012855.2:g.498753G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1629G= MANE Plus Clinical ENSP00000346701.4:p.Glu543=
ENST00000367255.10:c.25095G= MANE Select ENSP00000356224.5:p.Glu8365=
ENST00000423061.6:c.24951G= ENSP00000396024.1:p.Glu8317=
ENST00000672154.1:c.497G=
ENST00000672169.1:c.830G=
ENST00000673173.1:c.891-3486G=
ENST00000673451.1:c.867G= ENSP00000500189.1:p.Glu289=
ENST00000341594.9:c.23880G= ENSP00000341887.6:p.Glu7960=
ENST00000347037.9:n.1843G=
ENST00000354674.4:c.1629G= ENSP00000346701.4:p.Glu543=
ENST00000367251.7:c.3930G= ENSP00000356220.3:p.Glu1310=
ENST00000367255.9:c.25095G= ENSP00000356224.5:p.Glu8365=
ENST00000367256.9:n.8787G=
ENST00000367257.8:c.3033G= ENSP00000356226.4:p.Glu1011=
ENST00000409694.6:n.8679G=
ENST00000423061.5:c.24951G= ENSP00000396024.1:p.Glu8317=
ENST00000460912.6:n.1709G=
ENST00000478916.5:n.4117G=
ENST00000536990.5:n.1932G=
ENST00000539504.5:c.1560G= ENSP00000441052.1:p.Glu520=
NM_033071.3:c.24951G= NP_149062.1:p.Glu8317=
NM_182961.3:c.25095G= NP_892006.3:p.Glu8365=
XM_006715407.1:c.25200G= XP_006715470.1:p.Glu8400=
XM_006715408.1:c.25188G= XP_006715471.1:p.Glu8396=
XM_006715409.1:c.25179G= XP_006715472.1:p.Glu8393=
XM_006715410.1:c.25200G= XP_006715473.1:p.Glu8400=
XM_006715411.1:c.25149G= XP_006715474.1:p.Glu8383=
XM_006715412.1:c.25185G= XP_006715475.1:p.Glu8395=
XM_006715413.1:c.25131G= XP_006715476.1:p.Glu8377=
XM_006715414.1:c.25128G= XP_006715477.1:p.Glu8376=
XM_006715415.1:c.25131G= XP_006715478.1:p.Glu8377=
XM_006715416.1:c.25116G= XP_006715479.1:p.Glu8372=
XM_006715417.1:c.25059G= XP_006715480.1:p.Glu8353=
XM_006715420.1:c.25047G= XP_006715483.1:p.Glu8349=
XM_006715421.1:c.25044G= XP_006715484.1:p.Glu8348=
XM_006715422.1:c.25041G= XP_006715485.1:p.Glu8347=
XM_006715423.1:c.25200G= XP_006715486.1:p.Glu8400=
XM_006715424.1:c.25200G= XP_006715487.1:p.Glu8400=
XM_006715425.1:c.25131G= XP_006715488.1:p.Glu8377=
XM_011535641.1:c.25197G= XP_011533943.1:p.Glu8399=
XM_011535642.1:c.25185G= XP_011533944.1:p.Glu8395=
XM_011535643.1:c.25035G= XP_011533945.1:p.Glu8345=
XM_011535644.1:c.23475G= XP_011533946.1:p.Glu7825=
XM_011535645.1:c.22968G= XP_011533947.1:p.Glu7656=
XM_011535647.1:c.18435G= XP_011533949.1:p.Glu6145=
NM_001347701.1:c.1701G= NP_001334630.1:p.Glu567=
NM_001347702.1:c.1629G= NP_001334631.1:p.Glu543=
XM_006715408.2:c.25188G= XP_006715471.1:p.Glu8396=
XM_006715410.2:c.25200G= XP_006715473.1:p.Glu8400=
XM_006715412.2:c.25185G= XP_006715475.1:p.Glu8395=
XM_006715413.2:c.25131G= XP_006715476.1:p.Glu8377=
XM_006715415.2:c.25131G= XP_006715478.1:p.Glu8377=
XM_006715416.2:c.25116G= XP_006715479.1:p.Glu8372=
XM_006715417.2:c.25059G= XP_006715480.1:p.Glu8353=
XM_006715420.2:c.25047G= XP_006715483.1:p.Glu8349=
XM_006715421.2:c.25044G= XP_006715484.1:p.Glu8348=
XM_006715423.2:c.25200G= XP_006715486.1:p.Glu8400=
XM_006715424.2:c.25200G= XP_006715487.1:p.Glu8400=
XM_006715425.2:c.25131G= XP_006715488.1:p.Glu8377=
XM_011535641.2:c.25197G= XP_011533943.1:p.Glu8399=
XM_011535642.2:c.25185G= XP_011533944.1:p.Glu8395=
XM_011535645.2:c.22968G= XP_011533947.1:p.Glu7656=
XM_017010608.1:c.25200G= XP_016866097.1:p.Glu8400=
XM_017010609.1:c.25200G= XP_016866098.1:p.Glu8400=
XM_017010610.1:c.25179G= XP_016866099.1:p.Glu8393=
XM_017010611.2:c.25173G= XP_016866100.1:p.Glu8391=
XM_017010612.1:c.25122G= XP_016866101.1:p.Glu8374=
XM_017010613.1:c.25128G= XP_016866102.1:p.Glu8376=
XM_017010614.1:c.25044G= XP_016866103.1:p.Glu8348=
XM_017010615.1:c.24975G= XP_016866104.1:p.Glu8325=
XM_017010616.1:c.25131G= XP_016866105.1:p.Glu8377=
XM_017010617.1:c.25128G= XP_016866106.1:p.Glu8376=
XM_017010618.1:c.25116G= XP_016866107.1:p.Glu8372=
XM_017010619.1:c.23475G= XP_016866108.1:p.Glu7825=
NM_182961.4:c.25095G= MANE Select NP_892006.3:p.Glu8365=
NM_001347701.2:c.1701G= NP_001334630.1:p.Glu567=
NM_001347702.2:c.1629G= MANE Plus Clinical NP_001334631.1:p.Glu543=
NM_033071.5:c.24951G= NP_149062.2:p.Glu8317=