Canonical Allele Identifier: CA366112945

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152230670C>T , CM000668.2:g.152230670C>T	GRCh38
NC_000006.11:g.152551805C>T , CM000668.1:g.152551805C>T	GRCh37
NC_000006.10:g.152593498C>T	NCBI36
NG_012855.1:g.411730G>A
NG_012855.2:g.411730G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_182961.4:c.21072G>A MANE Select	NP_892006.3:p.Trp7024Ter
ENST00000367255.10:c.21072G>A MANE Select	ENSP00000356224.5:p.Trp7024Ter
NM_033071.3:c.20859G>A	NP_149062.1:p.Trp6953Ter
NM_033071.5:c.20859G>A	NP_149062.2:p.Trp6953Ter
NM_182961.3:c.21072G>A	NP_892006.3:p.Trp7024Ter
ENST00000341594.9:c.19857G>A	ENSP00000341887.6:p.Trp6619Ter
ENST00000367255.9:c.21072G>A	ENSP00000356224.5:p.Trp7024Ter
ENST00000367256.9:n.4764G>A
ENST00000409694.6:n.4656G>A
ENST00000423061.5:c.20859G>A	ENSP00000396024.1:p.Trp6953Ter
ENST00000423061.6:c.20859G>A	ENSP00000396024.1:p.Trp6953Ter
XM_006715407.1:c.21108G>A	XP_006715470.1:p.Trp7036Ter
XM_006715408.1:c.21096G>A	XP_006715471.1:p.Trp7032Ter
XM_006715408.2:c.21096G>A	XP_006715471.1:p.Trp7032Ter
XM_006715409.1:c.21087G>A	XP_006715472.1:p.Trp7029Ter
XM_006715410.1:c.21108G>A	XP_006715473.1:p.Trp7036Ter
XM_006715410.2:c.21108G>A	XP_006715473.1:p.Trp7036Ter
XM_006715411.1:c.21057G>A	XP_006715474.1:p.Trp7019Ter
XM_006715412.1:c.21093G>A	XP_006715475.1:p.Trp7031Ter
XM_006715412.2:c.21093G>A	XP_006715475.1:p.Trp7031Ter
XM_006715413.1:c.21108G>A	XP_006715476.1:p.Trp7036Ter
XM_006715413.2:c.21108G>A	XP_006715476.1:p.Trp7036Ter
XM_006715414.1:c.21036G>A	XP_006715477.1:p.Trp7012Ter
XM_006715415.1:c.21108G>A	XP_006715478.1:p.Trp7036Ter
XM_006715415.2:c.21108G>A	XP_006715478.1:p.Trp7036Ter
XM_006715416.1:c.21093G>A	XP_006715479.1:p.Trp7031Ter
XM_006715416.2:c.21093G>A	XP_006715479.1:p.Trp7031Ter
XM_006715417.1:c.20967G>A	XP_006715480.1:p.Trp6989Ter
XM_006715417.2:c.20967G>A	XP_006715480.1:p.Trp6989Ter
XM_006715420.1:c.20955G>A	XP_006715483.1:p.Trp6985Ter
XM_006715420.2:c.20955G>A	XP_006715483.1:p.Trp6985Ter
XM_006715421.1:c.20952G>A	XP_006715484.1:p.Trp6984Ter
XM_006715421.2:c.20952G>A	XP_006715484.1:p.Trp6984Ter
XM_006715422.1:c.20949G>A	XP_006715485.1:p.Trp6983Ter
XM_006715423.1:c.21108G>A	XP_006715486.1:p.Trp7036Ter
XM_006715423.2:c.21108G>A	XP_006715486.1:p.Trp7036Ter
XM_006715424.1:c.21108G>A	XP_006715487.1:p.Trp7036Ter
XM_006715424.2:c.21108G>A	XP_006715487.1:p.Trp7036Ter
XM_006715425.1:c.21108G>A	XP_006715488.1:p.Trp7036Ter
XM_006715425.2:c.21108G>A	XP_006715488.1:p.Trp7036Ter
XM_011535641.1:c.21105G>A	XP_011533943.1:p.Trp7035Ter
XM_011535641.2:c.21105G>A	XP_011533943.1:p.Trp7035Ter
XM_011535642.1:c.21093G>A	XP_011533944.1:p.Trp7031Ter
XM_011535642.2:c.21093G>A	XP_011533944.1:p.Trp7031Ter
XM_011535643.1:c.20943G>A	XP_011533945.1:p.Trp6981Ter
XM_011535644.1:c.19383G>A	XP_011533946.1:p.Trp6461Ter
XM_011535645.1:c.18876G>A	XP_011533947.1:p.Trp6292Ter
XM_011535645.2:c.18876G>A	XP_011533947.1:p.Trp6292Ter
XM_011535647.1:c.14343G>A	XP_011533949.1:p.Trp4781Ter
XM_017010608.1:c.21108G>A	XP_016866097.1:p.Trp7036Ter
XM_017010609.1:c.21108G>A	XP_016866098.1:p.Trp7036Ter
XM_017010610.1:c.21087G>A	XP_016866099.1:p.Trp7029Ter
XM_017010611.2:c.21081G>A	XP_016866100.1:p.Trp7027Ter
XM_017010612.1:c.21030G>A	XP_016866101.1:p.Trp7010Ter
XM_017010613.1:c.21105G>A	XP_016866102.1:p.Trp7035Ter
XM_017010614.1:c.20952G>A	XP_016866103.1:p.Trp6984Ter
XM_017010615.1:c.20952G>A	XP_016866104.1:p.Trp6984Ter
XM_017010616.1:c.21108G>A	XP_016866105.1:p.Trp7036Ter
XM_017010617.1:c.21105G>A	XP_016866106.1:p.Trp7035Ter
XM_017010618.1:c.21093G>A	XP_016866107.1:p.Trp7031Ter
XM_017010619.1:c.19383G>A	XP_016866108.1:p.Trp6461Ter