Canonical Allele Identifier: CA1673188631

Gene: SYNE1 ESR1

Linked Data

• dbSNP Id: rs771432556

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152122411C>T , CM000668.2:g.152122411C>T	GRCh38
NC_000006.11:g.152443546C>T , CM000668.1:g.152443546C>T	GRCh37
NC_000006.10:g.152485239C>T	NCBI36
NG_012855.1:g.519989G>A
NG_008493.2:g.470721C>T
NG_012855.2:g.519989G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.*25G>A (SYNE1) MANE Plus Clinical	ENSP00000346701.4:n.*25G>A
ENST00000367255.10:c.*25G>A (SYNE1) MANE Select	ENSP00000356224.5:n.*25G>A
ENST00000423061.6:c.*25G>A (SYNE1)	ENSP00000396024.1:n.*25G>A
ENST00000672154.1:c.1762G>A (SYNE1)
ENST00000672169.1:c.2137G>A (SYNE1)
ENST00000673173.1:c.2004G>A (SYNE1)
ENST00000673451.1:c.2269G>A (SYNE1)	ENSP00000500189.1:n.2269G>A
ENST00000341594.9:c.*25G>A (SYNE1)	ENSP00000341887.6:n.*25G>A
ENST00000347037.9:n.3167G>A (SYNE1)
ENST00000354674.4:c.*25G>A (SYNE1)	ENSP00000346701.4:n.*25G>A
ENST00000367251.7:c.5195G>A (SYNE1)	ENSP00000356220.3:n.5195G>A
ENST00000367255.9:c.*25G>A (SYNE1)	ENSP00000356224.5:n.*25G>A
ENST00000367256.9:n.10111G>A (SYNE1)
ENST00000367257.8:c.4298G>A (SYNE1)	ENSP00000356226.4:n.4298G>A
ENST00000409694.6:n.10003G>A (SYNE1)
ENST00000423061.5:c.*25G>A (SYNE1)	ENSP00000396024.1:n.*25G>A
ENST00000427531.6:c.851-2855C>T (ESR1)	ENSP00000394721.2:n.851-2855C>T
ENST00000460912.6:n.3033G>A (SYNE1)
ENST00000478916.5:n.7056G>A (SYNE1)
ENST00000539504.5:c.*25G>A (SYNE1)	ENSP00000441052.1:n.*25G>A
NM_033071.3:c.*25G>A (SYNE1)	NP_149062.1:n.*25G>A
NM_182961.3:c.*25G>A (SYNE1)	NP_892006.3:n.*25G>A
XM_006715407.1:c.*25G>A (SYNE1)	XP_006715470.1:n.*25G>A
XM_006715408.1:c.*25G>A (SYNE1)	XP_006715471.1:n.*25G>A
XM_006715409.1:c.*25G>A (SYNE1)	XP_006715472.1:n.*25G>A
XM_006715410.1:c.*25G>A (SYNE1)	XP_006715473.1:n.*25G>A
XM_006715411.1:c.*25G>A (SYNE1)	XP_006715474.1:n.*25G>A
XM_006715412.1:c.*25G>A (SYNE1)	XP_006715475.1:n.*25G>A
XM_006715413.1:c.*25G>A (SYNE1)	XP_006715476.1:n.*25G>A
XM_006715414.1:c.*25G>A (SYNE1)	XP_006715477.1:n.*25G>A
XM_006715415.1:c.*25G>A (SYNE1)	XP_006715478.1:n.*25G>A
XM_006715416.1:c.*25G>A (SYNE1)	XP_006715479.1:n.*25G>A
XM_006715417.1:c.*25G>A (SYNE1)	XP_006715480.1:n.*25G>A
XM_006715420.1:c.*25G>A (SYNE1)	XP_006715483.1:n.*25G>A
XM_006715421.1:c.*25G>A (SYNE1)	XP_006715484.1:n.*25G>A
XM_006715422.1:c.*25G>A (SYNE1)	XP_006715485.1:n.*25G>A
XM_006715423.1:c.*230G>A (SYNE1)	XP_006715486.1:n.*230G>A
XM_006715424.1:c.*230G>A (SYNE1)	XP_006715487.1:n.*230G>A
XM_006715425.1:c.*230G>A (SYNE1)	XP_006715488.1:n.*230G>A
XM_011535641.1:c.*25G>A (SYNE1)	XP_011533943.1:n.*25G>A
XM_011535642.1:c.*25G>A (SYNE1)	XP_011533944.1:n.*25G>A
XM_011535643.1:c.*25G>A (SYNE1)	XP_011533945.1:n.*25G>A
XM_011535644.1:c.*25G>A (SYNE1)	XP_011533946.1:n.*25G>A
XM_011535645.1:c.*25G>A (SYNE1)	XP_011533947.1:n.*25G>A
XM_011535647.1:c.19801G>A (SYNE1)	XP_011533949.1:n.19801G>A
NM_001328100.1:c.851-2855C>T (ESR1)	NP_001315029.1:n.851-2855C>T
NM_001347701.1:c.*230G>A (SYNE1)	NP_001334630.1:n.*230G>A
NM_001347702.1:c.*25G>A (SYNE1)	NP_001334631.1:n.*25G>A
XM_006715408.2:c.*25G>A (SYNE1)	XP_006715471.1:n.*25G>A
XM_006715410.2:c.*25G>A (SYNE1)	XP_006715473.1:n.*25G>A
XM_006715412.2:c.*25G>A (SYNE1)	XP_006715475.1:n.*25G>A
XM_006715413.2:c.*25G>A (SYNE1)	XP_006715476.1:n.*25G>A
XM_006715415.2:c.*25G>A (SYNE1)	XP_006715478.1:n.*25G>A
XM_006715416.2:c.*25G>A (SYNE1)	XP_006715479.1:n.*25G>A
XM_006715417.2:c.*25G>A (SYNE1)	XP_006715480.1:n.*25G>A
XM_006715420.2:c.*25G>A (SYNE1)	XP_006715483.1:n.*25G>A
XM_006715421.2:c.*25G>A (SYNE1)	XP_006715484.1:n.*25G>A
XM_006715423.2:c.*230G>A (SYNE1)	XP_006715486.1:n.*230G>A
XM_006715424.2:c.*230G>A (SYNE1)	XP_006715487.1:n.*230G>A
XM_006715425.2:c.*230G>A (SYNE1)	XP_006715488.1:n.*230G>A
XM_011535641.2:c.*25G>A (SYNE1)	XP_011533943.1:n.*25G>A
XM_011535642.2:c.*25G>A (SYNE1)	XP_011533944.1:n.*25G>A
XM_011535645.2:c.*25G>A (SYNE1)	XP_011533947.1:n.*25G>A
XM_017010608.1:c.*25G>A (SYNE1)	XP_016866097.1:n.*25G>A
XM_017010609.1:c.*25G>A (SYNE1)	XP_016866098.1:n.*25G>A
XM_017010610.1:c.*25G>A (SYNE1)	XP_016866099.1:n.*25G>A
XM_017010611.2:c.*25G>A (SYNE1)	XP_016866100.1:n.*25G>A
XM_017010612.1:c.*25G>A (SYNE1)	XP_016866101.1:n.*25G>A
XM_017010613.1:c.*25G>A (SYNE1)	XP_016866102.1:n.*25G>A
XM_017010614.1:c.*25G>A (SYNE1)	XP_016866103.1:n.*25G>A
XM_017010615.1:c.*25G>A (SYNE1)	XP_016866104.1:n.*25G>A
XM_017010616.1:c.*230G>A (SYNE1)	XP_016866105.1:n.*230G>A
XM_017010617.1:c.*230G>A (SYNE1)	XP_016866106.1:n.*230G>A
XM_017010618.1:c.*230G>A (SYNE1)	XP_016866107.1:n.*230G>A
XM_017010619.1:c.*25G>A (SYNE1)	XP_016866108.1:n.*25G>A
NM_182961.4:c.*25G>A (SYNE1) MANE Select	NP_892006.3:n.*25G>A
NM_001328100.2:c.851-2855C>T (ESR1)	NP_001315029.1:n.851-2855C>T
NM_001347701.2:c.*230G>A (SYNE1)	NP_001334630.1:n.*230G>A
NM_001347702.2:c.*25G>A (SYNE1) MANE Plus Clinical	NP_001334631.1:n.*25G>A
NM_033071.5:c.*25G>A (SYNE1)	NP_149062.2:n.*25G>A