Canonical Allele Identifier: CA1673206170
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152139983G= , CM000668.2:g.152139983G= GRCh38
NC_000006.11:g.152461118G= , CM000668.1:g.152461118G= GRCh37
NC_000006.10:g.152502811G= NCBI36
NG_012855.1:g.502417C=
NG_012855.2:g.502417C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1959C= MANE Plus Clinical ENSP00000346701.4:p.Ile653=
ENST00000367255.10:c.25425C= MANE Select ENSP00000356224.5:p.Ile8475=
ENST00000423061.6:c.25281C= ENSP00000396024.1:p.Ile8427=
ENST00000672154.1:c.827C=
ENST00000672169.1:c.1160C=
ENST00000673173.1:c.1069C=
ENST00000673451.1:c.1197C= ENSP00000500189.1:p.Ile399=
ENST00000341594.9:c.24210C= ENSP00000341887.6:p.Ile8070=
ENST00000347037.9:n.2173C=
ENST00000354674.4:c.1959C= ENSP00000346701.4:p.Ile653=
ENST00000367251.7:c.4260C= ENSP00000356220.3:p.Ile1420=
ENST00000367255.9:c.25425C= ENSP00000356224.5:p.Ile8475=
ENST00000367256.9:n.9117C=
ENST00000367257.8:c.3363C= ENSP00000356226.4:p.Ile1121=
ENST00000409694.6:n.9009C=
ENST00000423061.5:c.25281C= ENSP00000396024.1:p.Ile8427=
ENST00000460912.6:n.2039C=
ENST00000478916.5:n.4447C=
ENST00000536990.5:n.2262C=
ENST00000539504.5:c.1890C= ENSP00000441052.1:p.Ile630=
NM_033071.3:c.25281C= NP_149062.1:p.Ile8427=
NM_182961.3:c.25425C= NP_892006.3:p.Ile8475=
XM_006715407.1:c.25530C= XP_006715470.1:p.Ile8510=
XM_006715408.1:c.25518C= XP_006715471.1:p.Ile8506=
XM_006715409.1:c.25509C= XP_006715472.1:p.Ile8503=
XM_006715410.1:c.25530C= XP_006715473.1:p.Ile8510=
XM_006715411.1:c.25479C= XP_006715474.1:p.Ile8493=
XM_006715412.1:c.25515C= XP_006715475.1:p.Ile8505=
XM_006715413.1:c.25461C= XP_006715476.1:p.Ile8487=
XM_006715414.1:c.25458C= XP_006715477.1:p.Ile8486=
XM_006715415.1:c.25461C= XP_006715478.1:p.Ile8487=
XM_006715416.1:c.25446C= XP_006715479.1:p.Ile8482=
XM_006715417.1:c.25389C= XP_006715480.1:p.Ile8463=
XM_006715420.1:c.25377C= XP_006715483.1:p.Ile8459=
XM_006715421.1:c.25374C= XP_006715484.1:p.Ile8458=
XM_006715422.1:c.25371C= XP_006715485.1:p.Ile8457=
XM_006715423.1:c.25530C= XP_006715486.1:p.Ile8510=
XM_006715424.1:c.25530C= XP_006715487.1:p.Ile8510=
XM_006715425.1:c.25461C= XP_006715488.1:p.Ile8487=
XM_011535641.1:c.25527C= XP_011533943.1:p.Ile8509=
XM_011535642.1:c.25515C= XP_011533944.1:p.Ile8505=
XM_011535643.1:c.25365C= XP_011533945.1:p.Ile8455=
XM_011535644.1:c.23805C= XP_011533946.1:p.Ile7935=
XM_011535645.1:c.23298C= XP_011533947.1:p.Ile7766=
XM_011535647.1:c.18765C= XP_011533949.1:p.Ile6255=
NM_001347701.1:c.2031C= NP_001334630.1:p.Ile677=
NM_001347702.1:c.1959C= NP_001334631.1:p.Ile653=
XM_006715408.2:c.25518C= XP_006715471.1:p.Ile8506=
XM_006715410.2:c.25530C= XP_006715473.1:p.Ile8510=
XM_006715412.2:c.25515C= XP_006715475.1:p.Ile8505=
XM_006715413.2:c.25461C= XP_006715476.1:p.Ile8487=
XM_006715415.2:c.25461C= XP_006715478.1:p.Ile8487=
XM_006715416.2:c.25446C= XP_006715479.1:p.Ile8482=
XM_006715417.2:c.25389C= XP_006715480.1:p.Ile8463=
XM_006715420.2:c.25377C= XP_006715483.1:p.Ile8459=
XM_006715421.2:c.25374C= XP_006715484.1:p.Ile8458=
XM_006715423.2:c.25530C= XP_006715486.1:p.Ile8510=
XM_006715424.2:c.25530C= XP_006715487.1:p.Ile8510=
XM_006715425.2:c.25461C= XP_006715488.1:p.Ile8487=
XM_011535641.2:c.25527C= XP_011533943.1:p.Ile8509=
XM_011535642.2:c.25515C= XP_011533944.1:p.Ile8505=
XM_011535645.2:c.23298C= XP_011533947.1:p.Ile7766=
XM_017010608.1:c.25530C= XP_016866097.1:p.Ile8510=
XM_017010609.1:c.25530C= XP_016866098.1:p.Ile8510=
XM_017010610.1:c.25509C= XP_016866099.1:p.Ile8503=
XM_017010611.2:c.25503C= XP_016866100.1:p.Ile8501=
XM_017010612.1:c.25452C= XP_016866101.1:p.Ile8484=
XM_017010613.1:c.25458C= XP_016866102.1:p.Ile8486=
XM_017010614.1:c.25374C= XP_016866103.1:p.Ile8458=
XM_017010615.1:c.25305C= XP_016866104.1:p.Ile8435=
XM_017010616.1:c.25461C= XP_016866105.1:p.Ile8487=
XM_017010617.1:c.25458C= XP_016866106.1:p.Ile8486=
XM_017010618.1:c.25446C= XP_016866107.1:p.Ile8482=
XM_017010619.1:c.23805C= XP_016866108.1:p.Ile7935=
NM_182961.4:c.25425C= MANE Select NP_892006.3:p.Ile8475=
NM_001347701.2:c.2031C= NP_001334630.1:p.Ile677=
NM_001347702.2:c.1959C= MANE Plus Clinical NP_001334631.1:p.Ile653=
NM_033071.5:c.25281C= NP_149062.2:p.Ile8427=