Canonical Allele Identifier: CA366089157

Gene: SYNE1 ESR1

Linked Data

• MyVariant Identifiers: chr6:g.152443764C>T (hg19) ; chr6:g.152122629C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152122629C>T , CM000668.2:g.152122629C>T	GRCh38
NC_000006.11:g.152443764C>T , CM000668.1:g.152443764C>T	GRCh37
NC_000006.10:g.152485457C>T	NCBI36
NG_012855.1:g.519771G>A
NG_008493.2:g.470939C>T
NG_012855.2:g.519771G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.2735G>A (SYNE1) MANE Plus Clinical	ENSP00000346701.4:p.Gly912Asp
ENST00000367255.10:c.26201G>A (SYNE1) MANE Select	ENSP00000356224.5:p.Gly8734Asp
ENST00000423061.6:c.26057G>A (SYNE1)	ENSP00000396024.1:p.Gly8686Asp
ENST00000672154.1:c.1544G>A (SYNE1)
ENST00000672169.1:c.1919G>A (SYNE1)
ENST00000673173.1:c.1786G>A (SYNE1)
ENST00000673451.1:c.2051G>A (SYNE1)	ENSP00000500189.1:n.2051G>A
ENST00000341594.9:c.24986G>A (SYNE1)	ENSP00000341887.6:p.Gly8329Asp
ENST00000347037.9:n.2949G>A (SYNE1)
ENST00000354674.4:c.2735G>A (SYNE1)	ENSP00000346701.4:p.Gly912Asp
ENST00000367251.7:c.4977G>A (SYNE1)	ENSP00000356220.3:n.4977G>A
ENST00000367255.9:c.26201G>A (SYNE1)	ENSP00000356224.5:p.Gly8734Asp
ENST00000367256.9:n.9893G>A (SYNE1)
ENST00000367257.8:c.4080G>A (SYNE1)	ENSP00000356226.4:n.4080G>A
ENST00000409694.6:n.9785G>A (SYNE1)
ENST00000423061.5:c.26057G>A (SYNE1)	ENSP00000396024.1:p.Gly8686Asp
ENST00000427531.6:c.851-2637C>T (ESR1)	ENSP00000394721.2:n.851-2637C>T
ENST00000460912.6:n.2815G>A (SYNE1)
ENST00000478916.5:n.6838G>A (SYNE1)
ENST00000536990.5:n.2979G>A (SYNE1)
ENST00000539504.5:c.2666G>A (SYNE1)	ENSP00000441052.1:p.Gly889Asp
NM_033071.3:c.26057G>A (SYNE1)	NP_149062.1:p.Gly8686Asp
NM_182961.3:c.26201G>A (SYNE1)	NP_892006.3:p.Gly8734Asp
XM_006715407.1:c.26348G>A (SYNE1)	XP_006715470.1:p.Gly8783Asp
XM_006715408.1:c.26336G>A (SYNE1)	XP_006715471.1:p.Gly8779Asp
XM_006715409.1:c.26327G>A (SYNE1)	XP_006715472.1:p.Gly8776Asp
XM_006715410.1:c.26306G>A (SYNE1)	XP_006715473.1:p.Gly8769Asp
XM_006715411.1:c.26297G>A (SYNE1)	XP_006715474.1:p.Gly8766Asp
XM_006715412.1:c.26291G>A (SYNE1)	XP_006715475.1:p.Gly8764Asp
XM_006715413.1:c.26279G>A (SYNE1)	XP_006715476.1:p.Gly8760Asp
XM_006715414.1:c.26276G>A (SYNE1)	XP_006715477.1:p.Gly8759Asp
XM_006715415.1:c.26237G>A (SYNE1)	XP_006715478.1:p.Gly8746Asp
XM_006715416.1:c.26222G>A (SYNE1)	XP_006715479.1:p.Gly8741Asp
XM_006715417.1:c.26207G>A (SYNE1)	XP_006715480.1:p.Gly8736Asp
XM_006715420.1:c.26195G>A (SYNE1)	XP_006715483.1:p.Gly8732Asp
XM_006715421.1:c.26192G>A (SYNE1)	XP_006715484.1:p.Gly8731Asp
XM_006715422.1:c.26189G>A (SYNE1)	XP_006715485.1:p.Gly8730Asp
XM_006715423.1:c.*12G>A (SYNE1)	XP_006715486.1:n.*12G>A
XM_006715424.1:c.*12G>A (SYNE1)	XP_006715487.1:n.*12G>A
XM_006715425.1:c.*12G>A (SYNE1)	XP_006715488.1:n.*12G>A
XM_011535641.1:c.26345G>A (SYNE1)	XP_011533943.1:p.Gly8782Asp
XM_011535642.1:c.26333G>A (SYNE1)	XP_011533944.1:p.Gly8778Asp
XM_011535643.1:c.26183G>A (SYNE1)	XP_011533945.1:p.Gly8728Asp
XM_011535644.1:c.24623G>A (SYNE1)	XP_011533946.1:p.Gly8208Asp
XM_011535645.1:c.24116G>A (SYNE1)	XP_011533947.1:p.Gly8039Asp
XM_011535647.1:c.19583G>A (SYNE1)	XP_011533949.1:p.Gly6528Asp
NM_001328100.1:c.851-2637C>T (ESR1)	NP_001315029.1:n.851-2637C>T
NM_001347701.1:c.*12G>A (SYNE1)	NP_001334630.1:n.*12G>A
NM_001347702.1:c.2735G>A (SYNE1)	NP_001334631.1:p.Gly912Asp
XM_006715408.2:c.26336G>A (SYNE1)	XP_006715471.1:p.Gly8779Asp
XM_006715410.2:c.26306G>A (SYNE1)	XP_006715473.1:p.Gly8769Asp
XM_006715412.2:c.26291G>A (SYNE1)	XP_006715475.1:p.Gly8764Asp
XM_006715413.2:c.26279G>A (SYNE1)	XP_006715476.1:p.Gly8760Asp
XM_006715415.2:c.26237G>A (SYNE1)	XP_006715478.1:p.Gly8746Asp
XM_006715416.2:c.26222G>A (SYNE1)	XP_006715479.1:p.Gly8741Asp
XM_006715417.2:c.26207G>A (SYNE1)	XP_006715480.1:p.Gly8736Asp
XM_006715420.2:c.26195G>A (SYNE1)	XP_006715483.1:p.Gly8732Asp
XM_006715421.2:c.26192G>A (SYNE1)	XP_006715484.1:p.Gly8731Asp
XM_006715423.2:c.*12G>A (SYNE1)	XP_006715486.1:n.*12G>A
XM_006715424.2:c.*12G>A (SYNE1)	XP_006715487.1:n.*12G>A
XM_006715425.2:c.*12G>A (SYNE1)	XP_006715488.1:n.*12G>A
XM_011535641.2:c.26345G>A (SYNE1)	XP_011533943.1:p.Gly8782Asp
XM_011535642.2:c.26333G>A (SYNE1)	XP_011533944.1:p.Gly8778Asp
XM_011535645.2:c.24116G>A (SYNE1)	XP_011533947.1:p.Gly8039Asp
XM_017010608.1:c.26348G>A (SYNE1)	XP_016866097.1:p.Gly8783Asp
XM_017010609.1:c.26348G>A (SYNE1)	XP_016866098.1:p.Gly8783Asp
XM_017010610.1:c.26327G>A (SYNE1)	XP_016866099.1:p.Gly8776Asp
XM_017010611.2:c.26321G>A (SYNE1)	XP_016866100.1:p.Gly8774Asp
XM_017010612.1:c.26270G>A (SYNE1)	XP_016866101.1:p.Gly8757Asp
XM_017010613.1:c.26234G>A (SYNE1)	XP_016866102.1:p.Gly8745Asp
XM_017010614.1:c.26192G>A (SYNE1)	XP_016866103.1:p.Gly8731Asp
XM_017010615.1:c.26081G>A (SYNE1)	XP_016866104.1:p.Gly8694Asp
XM_017010616.1:c.*12G>A (SYNE1)	XP_016866105.1:n.*12G>A
XM_017010617.1:c.*12G>A (SYNE1)	XP_016866106.1:n.*12G>A
XM_017010618.1:c.*12G>A (SYNE1)	XP_016866107.1:n.*12G>A
XM_017010619.1:c.24623G>A (SYNE1)	XP_016866108.1:p.Gly8208Asp
NM_182961.4:c.26201G>A (SYNE1) MANE Select	NP_892006.3:p.Gly8734Asp
NM_001328100.2:c.851-2637C>T (ESR1)	NP_001315029.1:n.851-2637C>T
NM_001347701.2:c.*12G>A (SYNE1)	NP_001334630.1:n.*12G>A
NM_001347702.2:c.2735G>A (SYNE1) MANE Plus Clinical	NP_001334631.1:p.Gly912Asp
NM_033071.5:c.26057G>A (SYNE1)	NP_149062.2:p.Gly8686Asp