Canonical Allele Identifier: CA366086883

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152473125T>G (hg19) ; chr6:g.152151990T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152151990T>G , CM000668.2:g.152151990T>G	GRCh38
NC_000006.11:g.152473125T>G , CM000668.1:g.152473125T>G	GRCh37
NC_000006.10:g.152514818T>G	NCBI36
NG_012855.1:g.490410A>C
NG_012855.2:g.490410A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354674.5:c.746A>C MANE Plus Clinical	ENSP00000346701.4:p.Lys249Thr
ENST00000367255.10:c.24281A>C MANE Select	ENSP00000356224.5:p.Lys8094Thr
ENST00000423061.6:c.24068A>C	ENSP00000396024.1:p.Lys8023Thr
ENST00000672169.1:c.16A>C
ENST00000673173.1:c.195A>C
ENST00000673451.1:c.53A>C	ENSP00000500189.1:p.Lys18Thr
ENST00000341594.9:c.23066A>C	ENSP00000341887.6:p.Lys7689Thr
ENST00000347037.9:n.960A>C
ENST00000354674.4:c.746A>C	ENSP00000346701.4:p.Lys249Thr
ENST00000367251.7:c.3047A>C	ENSP00000356220.3:p.Lys1016Thr
ENST00000367255.9:c.24281A>C	ENSP00000356224.5:p.Lys8094Thr
ENST00000367256.9:n.7973A>C
ENST00000367257.8:c.2219A>C	ENSP00000356226.4:p.Lys740Thr
ENST00000409694.6:n.7865A>C
ENST00000423061.5:c.24068A>C	ENSP00000396024.1:p.Lys8023Thr
ENST00000460912.6:n.826A>C
ENST00000476519.1:n.343A>C
ENST00000536990.5:n.1118A>C
ENST00000539504.5:c.746A>C	ENSP00000441052.1:p.Lys249Thr
NM_033071.3:c.24068A>C	NP_149062.1:p.Lys8023Thr
NM_182961.3:c.24281A>C	NP_892006.3:p.Lys8094Thr
XM_006715407.1:c.24317A>C	XP_006715470.1:p.Lys8106Thr
XM_006715408.1:c.24305A>C	XP_006715471.1:p.Lys8102Thr
XM_006715409.1:c.24296A>C	XP_006715472.1:p.Lys8099Thr
XM_006715410.1:c.24317A>C	XP_006715473.1:p.Lys8106Thr
XM_006715411.1:c.24266A>C	XP_006715474.1:p.Lys8089Thr
XM_006715412.1:c.24302A>C	XP_006715475.1:p.Lys8101Thr
XM_006715413.1:c.24317A>C	XP_006715476.1:p.Lys8106Thr
XM_006715414.1:c.24245A>C	XP_006715477.1:p.Lys8082Thr
XM_006715415.1:c.24317A>C	XP_006715478.1:p.Lys8106Thr
XM_006715416.1:c.24302A>C	XP_006715479.1:p.Lys8101Thr
XM_006715417.1:c.24176A>C	XP_006715480.1:p.Lys8059Thr
XM_006715420.1:c.24164A>C	XP_006715483.1:p.Lys8055Thr
XM_006715421.1:c.24161A>C	XP_006715484.1:p.Lys8054Thr
XM_006715422.1:c.24158A>C	XP_006715485.1:p.Lys8053Thr
XM_006715423.1:c.24317A>C	XP_006715486.1:p.Lys8106Thr
XM_006715424.1:c.24317A>C	XP_006715487.1:p.Lys8106Thr
XM_006715425.1:c.24317A>C	XP_006715488.1:p.Lys8106Thr
XM_011535641.1:c.24314A>C	XP_011533943.1:p.Lys8105Thr
XM_011535642.1:c.24302A>C	XP_011533944.1:p.Lys8101Thr
XM_011535643.1:c.24152A>C	XP_011533945.1:p.Lys8051Thr
XM_011535644.1:c.22592A>C	XP_011533946.1:p.Lys7531Thr
XM_011535645.1:c.22085A>C	XP_011533947.1:p.Lys7362Thr
XM_011535647.1:c.17552A>C	XP_011533949.1:p.Lys5851Thr
NM_001347701.1:c.887A>C	NP_001334630.1:p.Lys296Thr
NM_001347702.1:c.746A>C	NP_001334631.1:p.Lys249Thr
XM_006715408.2:c.24305A>C	XP_006715471.1:p.Lys8102Thr
XM_006715410.2:c.24317A>C	XP_006715473.1:p.Lys8106Thr
XM_006715412.2:c.24302A>C	XP_006715475.1:p.Lys8101Thr
XM_006715413.2:c.24317A>C	XP_006715476.1:p.Lys8106Thr
XM_006715415.2:c.24317A>C	XP_006715478.1:p.Lys8106Thr
XM_006715416.2:c.24302A>C	XP_006715479.1:p.Lys8101Thr
XM_006715417.2:c.24176A>C	XP_006715480.1:p.Lys8059Thr
XM_006715420.2:c.24164A>C	XP_006715483.1:p.Lys8055Thr
XM_006715421.2:c.24161A>C	XP_006715484.1:p.Lys8054Thr
XM_006715423.2:c.24317A>C	XP_006715486.1:p.Lys8106Thr
XM_006715424.2:c.24317A>C	XP_006715487.1:p.Lys8106Thr
XM_006715425.2:c.24317A>C	XP_006715488.1:p.Lys8106Thr
XM_011535641.2:c.24314A>C	XP_011533943.1:p.Lys8105Thr
XM_011535642.2:c.24302A>C	XP_011533944.1:p.Lys8101Thr
XM_011535645.2:c.22085A>C	XP_011533947.1:p.Lys7362Thr
XM_017010608.1:c.24317A>C	XP_016866097.1:p.Lys8106Thr
XM_017010609.1:c.24317A>C	XP_016866098.1:p.Lys8106Thr
XM_017010610.1:c.24296A>C	XP_016866099.1:p.Lys8099Thr
XM_017010611.2:c.24290A>C	XP_016866100.1:p.Lys8097Thr
XM_017010612.1:c.24239A>C	XP_016866101.1:p.Lys8080Thr
XM_017010613.1:c.24314A>C	XP_016866102.1:p.Lys8105Thr
XM_017010614.1:c.24161A>C	XP_016866103.1:p.Lys8054Thr
XM_017010615.1:c.24161A>C	XP_016866104.1:p.Lys8054Thr
XM_017010616.1:c.24317A>C	XP_016866105.1:p.Lys8106Thr
XM_017010617.1:c.24314A>C	XP_016866106.1:p.Lys8105Thr
XM_017010618.1:c.24302A>C	XP_016866107.1:p.Lys8101Thr
XM_017010619.1:c.22592A>C	XP_016866108.1:p.Lys7531Thr
NM_182961.4:c.24281A>C MANE Select	NP_892006.3:p.Lys8094Thr
NM_001347701.2:c.887A>C	NP_001334630.1:p.Lys296Thr
NM_001347702.2:c.746A>C MANE Plus Clinical	NP_001334631.1:p.Lys249Thr
NM_033071.5:c.24068A>C	NP_149062.2:p.Lys8023Thr