Canonical Allele Identifier: CA366088740

Gene: SYNE1 ESR1

Linked Data

• MyVariant Identifiers: chr6:g.152443656T>A (hg19) ; chr6:g.152122521T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152122521T>A , CM000668.2:g.152122521T>A	GRCh38
NC_000006.11:g.152443656T>A , CM000668.1:g.152443656T>A	GRCh37
NC_000006.10:g.152485349T>A	NCBI36
NG_012855.1:g.519879A>T
NG_008493.2:g.470831T>A
NG_012855.2:g.519879A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.2843A>T (SYNE1) MANE Plus Clinical	ENSP00000346701.4:p.Glu948Val
ENST00000367255.10:c.26309A>T (SYNE1) MANE Select	ENSP00000356224.5:p.Glu8770Val
ENST00000423061.6:c.26165A>T (SYNE1)	ENSP00000396024.1:p.Glu8722Val
ENST00000672154.1:c.1652A>T (SYNE1)
ENST00000672169.1:c.2027A>T (SYNE1)
ENST00000673173.1:c.1894A>T (SYNE1)
ENST00000673451.1:c.2159A>T (SYNE1)	ENSP00000500189.1:n.2159A>T
ENST00000341594.9:c.25094A>T (SYNE1)	ENSP00000341887.6:p.Glu8365Val
ENST00000347037.9:n.3057A>T (SYNE1)
ENST00000354674.4:c.2843A>T (SYNE1)	ENSP00000346701.4:p.Glu948Val
ENST00000367251.7:c.5085A>T (SYNE1)	ENSP00000356220.3:n.5085A>T
ENST00000367255.9:c.26309A>T (SYNE1)	ENSP00000356224.5:p.Glu8770Val
ENST00000367256.9:n.10001A>T (SYNE1)
ENST00000367257.8:c.4188A>T (SYNE1)	ENSP00000356226.4:n.4188A>T
ENST00000409694.6:n.9893A>T (SYNE1)
ENST00000423061.5:c.26165A>T (SYNE1)	ENSP00000396024.1:p.Glu8722Val
ENST00000427531.6:c.851-2745T>A (ESR1)	ENSP00000394721.2:n.851-2745T>A
ENST00000460912.6:n.2923A>T (SYNE1)
ENST00000478916.5:n.6946A>T (SYNE1)
ENST00000539504.5:c.2774A>T (SYNE1)	ENSP00000441052.1:p.Glu925Val
NM_033071.3:c.26165A>T (SYNE1)	NP_149062.1:p.Glu8722Val
NM_182961.3:c.26309A>T (SYNE1)	NP_892006.3:p.Glu8770Val
XM_006715407.1:c.26456A>T (SYNE1)	XP_006715470.1:p.Glu8819Val
XM_006715408.1:c.26444A>T (SYNE1)	XP_006715471.1:p.Glu8815Val
XM_006715409.1:c.26435A>T (SYNE1)	XP_006715472.1:p.Glu8812Val
XM_006715410.1:c.26414A>T (SYNE1)	XP_006715473.1:p.Glu8805Val
XM_006715411.1:c.26405A>T (SYNE1)	XP_006715474.1:p.Glu8802Val
XM_006715412.1:c.26399A>T (SYNE1)	XP_006715475.1:p.Glu8800Val
XM_006715413.1:c.26387A>T (SYNE1)	XP_006715476.1:p.Glu8796Val
XM_006715414.1:c.26384A>T (SYNE1)	XP_006715477.1:p.Glu8795Val
XM_006715415.1:c.26345A>T (SYNE1)	XP_006715478.1:p.Glu8782Val
XM_006715416.1:c.26330A>T (SYNE1)	XP_006715479.1:p.Glu8777Val
XM_006715417.1:c.26315A>T (SYNE1)	XP_006715480.1:p.Glu8772Val
XM_006715420.1:c.26303A>T (SYNE1)	XP_006715483.1:p.Glu8768Val
XM_006715421.1:c.26300A>T (SYNE1)	XP_006715484.1:p.Glu8767Val
XM_006715422.1:c.26297A>T (SYNE1)	XP_006715485.1:p.Glu8766Val
XM_006715423.1:c.*120A>T (SYNE1)	XP_006715486.1:n.*120A>T
XM_006715424.1:c.*120A>T (SYNE1)	XP_006715487.1:n.*120A>T
XM_006715425.1:c.*120A>T (SYNE1)	XP_006715488.1:n.*120A>T
XM_011535641.1:c.26453A>T (SYNE1)	XP_011533943.1:p.Glu8818Val
XM_011535642.1:c.26441A>T (SYNE1)	XP_011533944.1:p.Glu8814Val
XM_011535643.1:c.26291A>T (SYNE1)	XP_011533945.1:p.Glu8764Val
XM_011535644.1:c.24731A>T (SYNE1)	XP_011533946.1:p.Glu8244Val
XM_011535645.1:c.24224A>T (SYNE1)	XP_011533947.1:p.Glu8075Val
XM_011535647.1:c.19691A>T (SYNE1)	XP_011533949.1:p.Glu6564Val
NM_001328100.1:c.851-2745T>A (ESR1)	NP_001315029.1:n.851-2745T>A
NM_001347701.1:c.*120A>T (SYNE1)	NP_001334630.1:n.*120A>T
NM_001347702.1:c.2843A>T (SYNE1)	NP_001334631.1:p.Glu948Val
XM_006715408.2:c.26444A>T (SYNE1)	XP_006715471.1:p.Glu8815Val
XM_006715410.2:c.26414A>T (SYNE1)	XP_006715473.1:p.Glu8805Val
XM_006715412.2:c.26399A>T (SYNE1)	XP_006715475.1:p.Glu8800Val
XM_006715413.2:c.26387A>T (SYNE1)	XP_006715476.1:p.Glu8796Val
XM_006715415.2:c.26345A>T (SYNE1)	XP_006715478.1:p.Glu8782Val
XM_006715416.2:c.26330A>T (SYNE1)	XP_006715479.1:p.Glu8777Val
XM_006715417.2:c.26315A>T (SYNE1)	XP_006715480.1:p.Glu8772Val
XM_006715420.2:c.26303A>T (SYNE1)	XP_006715483.1:p.Glu8768Val
XM_006715421.2:c.26300A>T (SYNE1)	XP_006715484.1:p.Glu8767Val
XM_006715423.2:c.*120A>T (SYNE1)	XP_006715486.1:n.*120A>T
XM_006715424.2:c.*120A>T (SYNE1)	XP_006715487.1:n.*120A>T
XM_006715425.2:c.*120A>T (SYNE1)	XP_006715488.1:n.*120A>T
XM_011535641.2:c.26453A>T (SYNE1)	XP_011533943.1:p.Glu8818Val
XM_011535642.2:c.26441A>T (SYNE1)	XP_011533944.1:p.Glu8814Val
XM_011535645.2:c.24224A>T (SYNE1)	XP_011533947.1:p.Glu8075Val
XM_017010608.1:c.26456A>T (SYNE1)	XP_016866097.1:p.Glu8819Val
XM_017010609.1:c.26456A>T (SYNE1)	XP_016866098.1:p.Glu8819Val
XM_017010610.1:c.26435A>T (SYNE1)	XP_016866099.1:p.Glu8812Val
XM_017010611.2:c.26429A>T (SYNE1)	XP_016866100.1:p.Glu8810Val
XM_017010612.1:c.26378A>T (SYNE1)	XP_016866101.1:p.Glu8793Val
XM_017010613.1:c.26342A>T (SYNE1)	XP_016866102.1:p.Glu8781Val
XM_017010614.1:c.26300A>T (SYNE1)	XP_016866103.1:p.Glu8767Val
XM_017010615.1:c.26189A>T (SYNE1)	XP_016866104.1:p.Glu8730Val
XM_017010616.1:c.*120A>T (SYNE1)	XP_016866105.1:n.*120A>T
XM_017010617.1:c.*120A>T (SYNE1)	XP_016866106.1:n.*120A>T
XM_017010618.1:c.*120A>T (SYNE1)	XP_016866107.1:n.*120A>T
XM_017010619.1:c.24731A>T (SYNE1)	XP_016866108.1:p.Glu8244Val
NM_182961.4:c.26309A>T (SYNE1) MANE Select	NP_892006.3:p.Glu8770Val
NM_001328100.2:c.851-2745T>A (ESR1)	NP_001315029.1:n.851-2745T>A
NM_001347701.2:c.*120A>T (SYNE1)	NP_001334630.1:n.*120A>T
NM_001347702.2:c.2843A>T (SYNE1) MANE Plus Clinical	NP_001334631.1:p.Glu948Val
NM_033071.5:c.26165A>T (SYNE1)	NP_149062.2:p.Glu8722Val