Canonical Allele Identifier: CA1673188903

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152122509C= , CM000668.2:g.152122509C= GRCh38
NC_000006.11:g.152443644C= , CM000668.1:g.152443644C= GRCh37
NC_000006.10:g.152485337C= NCBI36
NG_012855.1:g.519891G=
NG_008493.2:g.470819C=
NG_012855.2:g.519891G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.2855G= (SYNE1) MANE Plus Clinical ENSP00000346701.4:p.Cys952=
ENST00000367255.10:c.26321G= (SYNE1) MANE Select ENSP00000356224.5:p.Cys8774=
ENST00000423061.6:c.26177G= (SYNE1) ENSP00000396024.1:p.Cys8726=
ENST00000672154.1:c.1664G= (SYNE1)
ENST00000672169.1:c.2039G= (SYNE1)
ENST00000673173.1:c.1906G= (SYNE1)
ENST00000673451.1:c.2171G= (SYNE1) ENSP00000500189.1:n.2171G=
ENST00000341594.9:c.25106G= (SYNE1) ENSP00000341887.6:p.Cys8369=
ENST00000347037.9:n.3069G= (SYNE1)
ENST00000354674.4:c.2855G= (SYNE1) ENSP00000346701.4:p.Cys952=
ENST00000367251.7:c.5097G= (SYNE1) ENSP00000356220.3:n.5097G=
ENST00000367255.9:c.26321G= (SYNE1) ENSP00000356224.5:p.Cys8774=
ENST00000367256.9:n.10013G= (SYNE1)
ENST00000367257.8:c.4200G= (SYNE1) ENSP00000356226.4:n.4200G=
ENST00000409694.6:n.9905G= (SYNE1)
ENST00000423061.5:c.26177G= (SYNE1) ENSP00000396024.1:p.Cys8726=
ENST00000427531.6:c.851-2757C= (ESR1) ENSP00000394721.2:n.851-2757C=
ENST00000460912.6:n.2935G= (SYNE1)
ENST00000478916.5:n.6958G= (SYNE1)
ENST00000539504.5:c.2786G= (SYNE1) ENSP00000441052.1:p.Cys929=
NM_033071.3:c.26177G= (SYNE1) NP_149062.1:p.Cys8726=
NM_182961.3:c.26321G= (SYNE1) NP_892006.3:p.Cys8774=
XM_006715407.1:c.26468G= (SYNE1) XP_006715470.1:p.Cys8823=
XM_006715408.1:c.26456G= (SYNE1) XP_006715471.1:p.Cys8819=
XM_006715409.1:c.26447G= (SYNE1) XP_006715472.1:p.Cys8816=
XM_006715410.1:c.26426G= (SYNE1) XP_006715473.1:p.Cys8809=
XM_006715411.1:c.26417G= (SYNE1) XP_006715474.1:p.Cys8806=
XM_006715412.1:c.26411G= (SYNE1) XP_006715475.1:p.Cys8804=
XM_006715413.1:c.26399G= (SYNE1) XP_006715476.1:p.Cys8800=
XM_006715414.1:c.26396G= (SYNE1) XP_006715477.1:p.Cys8799=
XM_006715415.1:c.26357G= (SYNE1) XP_006715478.1:p.Cys8786=
XM_006715416.1:c.26342G= (SYNE1) XP_006715479.1:p.Cys8781=
XM_006715417.1:c.26327G= (SYNE1) XP_006715480.1:p.Cys8776=
XM_006715420.1:c.26315G= (SYNE1) XP_006715483.1:p.Cys8772=
XM_006715421.1:c.26312G= (SYNE1) XP_006715484.1:p.Cys8771=
XM_006715422.1:c.26309G= (SYNE1) XP_006715485.1:p.Cys8770=
XM_006715423.1:c.*132G= (SYNE1) XP_006715486.1:n.*132G=
XM_006715424.1:c.*132G= (SYNE1) XP_006715487.1:n.*132G=
XM_006715425.1:c.*132G= (SYNE1) XP_006715488.1:n.*132G=
XM_011535641.1:c.26465G= (SYNE1) XP_011533943.1:p.Cys8822=
XM_011535642.1:c.26453G= (SYNE1) XP_011533944.1:p.Cys8818=
XM_011535643.1:c.26303G= (SYNE1) XP_011533945.1:p.Cys8768=
XM_011535644.1:c.24743G= (SYNE1) XP_011533946.1:p.Cys8248=
XM_011535645.1:c.24236G= (SYNE1) XP_011533947.1:p.Cys8079=
XM_011535647.1:c.19703G= (SYNE1) XP_011533949.1:p.Cys6568=
NM_001328100.1:c.851-2757C= (ESR1) NP_001315029.1:n.851-2757C=
NM_001347701.1:c.*132G= (SYNE1) NP_001334630.1:n.*132G=
NM_001347702.1:c.2855G= (SYNE1) NP_001334631.1:p.Cys952=
XM_006715408.2:c.26456G= (SYNE1) XP_006715471.1:p.Cys8819=
XM_006715410.2:c.26426G= (SYNE1) XP_006715473.1:p.Cys8809=
XM_006715412.2:c.26411G= (SYNE1) XP_006715475.1:p.Cys8804=
XM_006715413.2:c.26399G= (SYNE1) XP_006715476.1:p.Cys8800=
XM_006715415.2:c.26357G= (SYNE1) XP_006715478.1:p.Cys8786=
XM_006715416.2:c.26342G= (SYNE1) XP_006715479.1:p.Cys8781=
XM_006715417.2:c.26327G= (SYNE1) XP_006715480.1:p.Cys8776=
XM_006715420.2:c.26315G= (SYNE1) XP_006715483.1:p.Cys8772=
XM_006715421.2:c.26312G= (SYNE1) XP_006715484.1:p.Cys8771=
XM_006715423.2:c.*132G= (SYNE1) XP_006715486.1:n.*132G=
XM_006715424.2:c.*132G= (SYNE1) XP_006715487.1:n.*132G=
XM_006715425.2:c.*132G= (SYNE1) XP_006715488.1:n.*132G=
XM_011535641.2:c.26465G= (SYNE1) XP_011533943.1:p.Cys8822=
XM_011535642.2:c.26453G= (SYNE1) XP_011533944.1:p.Cys8818=
XM_011535645.2:c.24236G= (SYNE1) XP_011533947.1:p.Cys8079=
XM_017010608.1:c.26468G= (SYNE1) XP_016866097.1:p.Cys8823=
XM_017010609.1:c.26468G= (SYNE1) XP_016866098.1:p.Cys8823=
XM_017010610.1:c.26447G= (SYNE1) XP_016866099.1:p.Cys8816=
XM_017010611.2:c.26441G= (SYNE1) XP_016866100.1:p.Cys8814=
XM_017010612.1:c.26390G= (SYNE1) XP_016866101.1:p.Cys8797=
XM_017010613.1:c.26354G= (SYNE1) XP_016866102.1:p.Cys8785=
XM_017010614.1:c.26312G= (SYNE1) XP_016866103.1:p.Cys8771=
XM_017010615.1:c.26201G= (SYNE1) XP_016866104.1:p.Cys8734=
XM_017010616.1:c.*132G= (SYNE1) XP_016866105.1:n.*132G=
XM_017010617.1:c.*132G= (SYNE1) XP_016866106.1:n.*132G=
XM_017010618.1:c.*132G= (SYNE1) XP_016866107.1:n.*132G=
XM_017010619.1:c.24743G= (SYNE1) XP_016866108.1:p.Cys8248=
NM_182961.4:c.26321G= (SYNE1) MANE Select NP_892006.3:p.Cys8774=
NM_001328100.2:c.851-2757C= (ESR1) NP_001315029.1:n.851-2757C=
NM_001347701.2:c.*132G= (SYNE1) NP_001334630.1:n.*132G=
NM_001347702.2:c.2855G= (SYNE1) MANE Plus Clinical NP_001334631.1:p.Cys952=
NM_033071.5:c.26177G= (SYNE1) NP_149062.2:p.Cys8726=