Canonical Allele Identifier: CA366088759

Gene: SYNE1 ESR1

Linked Data

• MyVariant Identifiers: chr6:g.152443659T>G (hg19) ; chr6:g.152122524T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152122524T>G , CM000668.2:g.152122524T>G	GRCh38
NC_000006.11:g.152443659T>G , CM000668.1:g.152443659T>G	GRCh37
NC_000006.10:g.152485352T>G	NCBI36
NG_012855.1:g.519876A>C
NG_008493.2:g.470834T>G
NG_012855.2:g.519876A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.2840A>C (SYNE1) MANE Plus Clinical	ENSP00000346701.4:p.Glu947Ala
ENST00000367255.10:c.26306A>C (SYNE1) MANE Select	ENSP00000356224.5:p.Glu8769Ala
ENST00000423061.6:c.26162A>C (SYNE1)	ENSP00000396024.1:p.Glu8721Ala
ENST00000672154.1:c.1649A>C (SYNE1)
ENST00000672169.1:c.2024A>C (SYNE1)
ENST00000673173.1:c.1891A>C (SYNE1)
ENST00000673451.1:c.2156A>C (SYNE1)	ENSP00000500189.1:n.2156A>C
ENST00000341594.9:c.25091A>C (SYNE1)	ENSP00000341887.6:p.Glu8364Ala
ENST00000347037.9:n.3054A>C (SYNE1)
ENST00000354674.4:c.2840A>C (SYNE1)	ENSP00000346701.4:p.Glu947Ala
ENST00000367251.7:c.5082A>C (SYNE1)	ENSP00000356220.3:n.5082A>C
ENST00000367255.9:c.26306A>C (SYNE1)	ENSP00000356224.5:p.Glu8769Ala
ENST00000367256.9:n.9998A>C (SYNE1)
ENST00000367257.8:c.4185A>C (SYNE1)	ENSP00000356226.4:n.4185A>C
ENST00000409694.6:n.9890A>C (SYNE1)
ENST00000423061.5:c.26162A>C (SYNE1)	ENSP00000396024.1:p.Glu8721Ala
ENST00000427531.6:c.851-2742T>G (ESR1)	ENSP00000394721.2:n.851-2742T>G
ENST00000460912.6:n.2920A>C (SYNE1)
ENST00000478916.5:n.6943A>C (SYNE1)
ENST00000539504.5:c.2771A>C (SYNE1)	ENSP00000441052.1:p.Glu924Ala
NM_033071.3:c.26162A>C (SYNE1)	NP_149062.1:p.Glu8721Ala
NM_182961.3:c.26306A>C (SYNE1)	NP_892006.3:p.Glu8769Ala
XM_006715407.1:c.26453A>C (SYNE1)	XP_006715470.1:p.Glu8818Ala
XM_006715408.1:c.26441A>C (SYNE1)	XP_006715471.1:p.Glu8814Ala
XM_006715409.1:c.26432A>C (SYNE1)	XP_006715472.1:p.Glu8811Ala
XM_006715410.1:c.26411A>C (SYNE1)	XP_006715473.1:p.Glu8804Ala
XM_006715411.1:c.26402A>C (SYNE1)	XP_006715474.1:p.Glu8801Ala
XM_006715412.1:c.26396A>C (SYNE1)	XP_006715475.1:p.Glu8799Ala
XM_006715413.1:c.26384A>C (SYNE1)	XP_006715476.1:p.Glu8795Ala
XM_006715414.1:c.26381A>C (SYNE1)	XP_006715477.1:p.Glu8794Ala
XM_006715415.1:c.26342A>C (SYNE1)	XP_006715478.1:p.Glu8781Ala
XM_006715416.1:c.26327A>C (SYNE1)	XP_006715479.1:p.Glu8776Ala
XM_006715417.1:c.26312A>C (SYNE1)	XP_006715480.1:p.Glu8771Ala
XM_006715420.1:c.26300A>C (SYNE1)	XP_006715483.1:p.Glu8767Ala
XM_006715421.1:c.26297A>C (SYNE1)	XP_006715484.1:p.Glu8766Ala
XM_006715422.1:c.26294A>C (SYNE1)	XP_006715485.1:p.Glu8765Ala
XM_006715423.1:c.*117A>C (SYNE1)	XP_006715486.1:n.*117A>C
XM_006715424.1:c.*117A>C (SYNE1)	XP_006715487.1:n.*117A>C
XM_006715425.1:c.*117A>C (SYNE1)	XP_006715488.1:n.*117A>C
XM_011535641.1:c.26450A>C (SYNE1)	XP_011533943.1:p.Glu8817Ala
XM_011535642.1:c.26438A>C (SYNE1)	XP_011533944.1:p.Glu8813Ala
XM_011535643.1:c.26288A>C (SYNE1)	XP_011533945.1:p.Glu8763Ala
XM_011535644.1:c.24728A>C (SYNE1)	XP_011533946.1:p.Glu8243Ala
XM_011535645.1:c.24221A>C (SYNE1)	XP_011533947.1:p.Glu8074Ala
XM_011535647.1:c.19688A>C (SYNE1)	XP_011533949.1:p.Glu6563Ala
NM_001328100.1:c.851-2742T>G (ESR1)	NP_001315029.1:n.851-2742T>G
NM_001347701.1:c.*117A>C (SYNE1)	NP_001334630.1:n.*117A>C
NM_001347702.1:c.2840A>C (SYNE1)	NP_001334631.1:p.Glu947Ala
XM_006715408.2:c.26441A>C (SYNE1)	XP_006715471.1:p.Glu8814Ala
XM_006715410.2:c.26411A>C (SYNE1)	XP_006715473.1:p.Glu8804Ala
XM_006715412.2:c.26396A>C (SYNE1)	XP_006715475.1:p.Glu8799Ala
XM_006715413.2:c.26384A>C (SYNE1)	XP_006715476.1:p.Glu8795Ala
XM_006715415.2:c.26342A>C (SYNE1)	XP_006715478.1:p.Glu8781Ala
XM_006715416.2:c.26327A>C (SYNE1)	XP_006715479.1:p.Glu8776Ala
XM_006715417.2:c.26312A>C (SYNE1)	XP_006715480.1:p.Glu8771Ala
XM_006715420.2:c.26300A>C (SYNE1)	XP_006715483.1:p.Glu8767Ala
XM_006715421.2:c.26297A>C (SYNE1)	XP_006715484.1:p.Glu8766Ala
XM_006715423.2:c.*117A>C (SYNE1)	XP_006715486.1:n.*117A>C
XM_006715424.2:c.*117A>C (SYNE1)	XP_006715487.1:n.*117A>C
XM_006715425.2:c.*117A>C (SYNE1)	XP_006715488.1:n.*117A>C
XM_011535641.2:c.26450A>C (SYNE1)	XP_011533943.1:p.Glu8817Ala
XM_011535642.2:c.26438A>C (SYNE1)	XP_011533944.1:p.Glu8813Ala
XM_011535645.2:c.24221A>C (SYNE1)	XP_011533947.1:p.Glu8074Ala
XM_017010608.1:c.26453A>C (SYNE1)	XP_016866097.1:p.Glu8818Ala
XM_017010609.1:c.26453A>C (SYNE1)	XP_016866098.1:p.Glu8818Ala
XM_017010610.1:c.26432A>C (SYNE1)	XP_016866099.1:p.Glu8811Ala
XM_017010611.2:c.26426A>C (SYNE1)	XP_016866100.1:p.Glu8809Ala
XM_017010612.1:c.26375A>C (SYNE1)	XP_016866101.1:p.Glu8792Ala
XM_017010613.1:c.26339A>C (SYNE1)	XP_016866102.1:p.Glu8780Ala
XM_017010614.1:c.26297A>C (SYNE1)	XP_016866103.1:p.Glu8766Ala
XM_017010615.1:c.26186A>C (SYNE1)	XP_016866104.1:p.Glu8729Ala
XM_017010616.1:c.*117A>C (SYNE1)	XP_016866105.1:n.*117A>C
XM_017010617.1:c.*117A>C (SYNE1)	XP_016866106.1:n.*117A>C
XM_017010618.1:c.*117A>C (SYNE1)	XP_016866107.1:n.*117A>C
XM_017010619.1:c.24728A>C (SYNE1)	XP_016866108.1:p.Glu8243Ala
NM_182961.4:c.26306A>C (SYNE1) MANE Select	NP_892006.3:p.Glu8769Ala
NM_001328100.2:c.851-2742T>G (ESR1)	NP_001315029.1:n.851-2742T>G
NM_001347701.2:c.*117A>C (SYNE1)	NP_001334630.1:n.*117A>C
NM_001347702.2:c.2840A>C (SYNE1) MANE Plus Clinical	NP_001334631.1:p.Glu947Ala
NM_033071.5:c.26162A>C (SYNE1)	NP_149062.2:p.Glu8721Ala