Canonical Allele Identifier: CA155442

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152132218T>C , CM000668.2:g.152132218T>C	GRCh38
NC_000006.11:g.152453353T>C , CM000668.1:g.152453353T>C	GRCh37
NC_000006.10:g.152495046T>C	NCBI36
NG_012855.1:g.510182A>G
NG_012855.2:g.510182A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.2536-4A>G MANE Plus Clinical	ENSP00000346701.4:n.2536-4A>G
ENST00000367255.10:c.26002-4A>G MANE Select	ENSP00000356224.5:n.26002-4A>G
ENST00000423061.6:c.25858-4A>G	ENSP00000396024.1:n.25858-4A>G
ENST00000672154.1:c.1404-4A>G
ENST00000672169.1:c.1779-4A>G
ENST00000673173.1:c.1646-4A>G
ENST00000673451.1:c.1852-4A>G	ENSP00000500189.1:n.1852-4A>G
ENST00000341594.9:c.24787-4A>G	ENSP00000341887.6:n.24787-4A>G
ENST00000347037.9:n.2750-4A>G
ENST00000354674.4:c.2536-4A>G	ENSP00000346701.4:n.2536-4A>G
ENST00000367251.7:c.4837-4A>G	ENSP00000356220.3:n.4837-4A>G
ENST00000367255.9:c.26002-4A>G	ENSP00000356224.5:n.26002-4A>G
ENST00000367256.9:n.9694-4A>G
ENST00000367257.8:c.3940-4A>G	ENSP00000356226.4:n.3940-4A>G
ENST00000409694.6:n.9586-4A>G
ENST00000423061.5:c.25858-4A>G	ENSP00000396024.1:n.25858-4A>G
ENST00000460912.6:n.2616-4A>G
ENST00000478916.5:n.6639-4A>G
ENST00000536990.5:n.2839-4A>G
ENST00000539504.5:c.2467-4A>G	ENSP00000441052.1:n.2467-4A>G
NM_033071.3:c.25858-4A>G	NP_149062.1:n.25858-4A>G
NM_182961.3:c.26002-4A>G	NP_892006.3:n.26002-4A>G
XM_006715407.1:c.26149-4A>G	XP_006715470.1:n.26149-4A>G
XM_006715408.1:c.26137-4A>G	XP_006715471.1:n.26137-4A>G
XM_006715409.1:c.26128-4A>G	XP_006715472.1:n.26128-4A>G
XM_006715410.1:c.26107-4A>G	XP_006715473.1:n.26107-4A>G
XM_006715411.1:c.26098-4A>G	XP_006715474.1:n.26098-4A>G
XM_006715412.1:c.26092-4A>G	XP_006715475.1:n.26092-4A>G
XM_006715413.1:c.26080-4A>G	XP_006715476.1:n.26080-4A>G
XM_006715414.1:c.26077-4A>G	XP_006715477.1:n.26077-4A>G
XM_006715415.1:c.26038-4A>G	XP_006715478.1:n.26038-4A>G
XM_006715416.1:c.26023-4A>G	XP_006715479.1:n.26023-4A>G
XM_006715417.1:c.26008-4A>G	XP_006715480.1:n.26008-4A>G
XM_006715420.1:c.25996-4A>G	XP_006715483.1:n.25996-4A>G
XM_006715421.1:c.25993-4A>G	XP_006715484.1:n.25993-4A>G
XM_006715422.1:c.25990-4A>G	XP_006715485.1:n.25990-4A>G
XM_006715423.1:c.26149-4A>G	XP_006715486.1:n.26149-4A>G
XM_006715424.1:c.26107-4A>G	XP_006715487.1:n.26107-4A>G
XM_006715425.1:c.26038-4A>G	XP_006715488.1:n.26038-4A>G
XM_011535641.1:c.26146-4A>G	XP_011533943.1:n.26146-4A>G
XM_011535642.1:c.26134-4A>G	XP_011533944.1:n.26134-4A>G
XM_011535643.1:c.25984-4A>G	XP_011533945.1:n.25984-4A>G
XM_011535644.1:c.24424-4A>G	XP_011533946.1:n.24424-4A>G
XM_011535645.1:c.23917-4A>G	XP_011533947.1:n.23917-4A>G
XM_011535647.1:c.19384-4A>G	XP_011533949.1:n.19384-4A>G
NM_001347701.1:c.2608-4A>G	NP_001334630.1:n.2608-4A>G
NM_001347702.1:c.2536-4A>G	NP_001334631.1:n.2536-4A>G
XM_006715408.2:c.26137-4A>G	XP_006715471.1:n.26137-4A>G
XM_006715410.2:c.26107-4A>G	XP_006715473.1:n.26107-4A>G
XM_006715412.2:c.26092-4A>G	XP_006715475.1:n.26092-4A>G
XM_006715413.2:c.26080-4A>G	XP_006715476.1:n.26080-4A>G
XM_006715415.2:c.26038-4A>G	XP_006715478.1:n.26038-4A>G
XM_006715416.2:c.26023-4A>G	XP_006715479.1:n.26023-4A>G
XM_006715417.2:c.26008-4A>G	XP_006715480.1:n.26008-4A>G
XM_006715420.2:c.25996-4A>G	XP_006715483.1:n.25996-4A>G
XM_006715421.2:c.25993-4A>G	XP_006715484.1:n.25993-4A>G
XM_006715423.2:c.26149-4A>G	XP_006715486.1:n.26149-4A>G
XM_006715424.2:c.26107-4A>G	XP_006715487.1:n.26107-4A>G
XM_006715425.2:c.26038-4A>G	XP_006715488.1:n.26038-4A>G
XM_011535641.2:c.26146-4A>G	XP_011533943.1:n.26146-4A>G
XM_011535642.2:c.26134-4A>G	XP_011533944.1:n.26134-4A>G
XM_011535645.2:c.23917-4A>G	XP_011533947.1:n.23917-4A>G
XM_017010608.1:c.26149-4A>G	XP_016866097.1:n.26149-4A>G
XM_017010609.1:c.26149-4A>G	XP_016866098.1:n.26149-4A>G
XM_017010610.1:c.26128-4A>G	XP_016866099.1:n.26128-4A>G
XM_017010611.2:c.26122-4A>G	XP_016866100.1:n.26122-4A>G
XM_017010612.1:c.26071-4A>G	XP_016866101.1:n.26071-4A>G
XM_017010613.1:c.26035-4A>G	XP_016866102.1:n.26035-4A>G
XM_017010614.1:c.25993-4A>G	XP_016866103.1:n.25993-4A>G
XM_017010615.1:c.25882-4A>G	XP_016866104.1:n.25882-4A>G
XM_017010616.1:c.26080-4A>G	XP_016866105.1:n.26080-4A>G
XM_017010617.1:c.26035-4A>G	XP_016866106.1:n.26035-4A>G
XM_017010618.1:c.26023-4A>G	XP_016866107.1:n.26023-4A>G
XM_017010619.1:c.24424-4A>G	XP_016866108.1:n.24424-4A>G
NM_182961.4:c.26002-4A>G MANE Select	NP_892006.3:n.26002-4A>G
NM_001347701.2:c.2608-4A>G	NP_001334630.1:n.2608-4A>G
NM_001347702.2:c.2536-4A>G MANE Plus Clinical	NP_001334631.1:n.2536-4A>G
NM_033071.5:c.25858-4A>G	NP_149062.2:n.25858-4A>G