Canonical Allele Identifier: CA452751269

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152554994G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152233859G>T , CM000668.2:g.152233859G>T	GRCh38
NC_000006.11:g.152554994G>T , CM000668.1:g.152554994G>T	GRCh37
NC_000006.10:g.152596687G>T	NCBI36
NG_012855.1:g.408541C>A
NG_012855.2:g.408541C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367255.10:c.20634C>A MANE Select	ENSP00000356224.5:p.Arg6878=
ENST00000423061.6:c.20421C>A	ENSP00000396024.1:p.Arg6807=
ENST00000341594.9:c.19419C>A	ENSP00000341887.6:p.Arg6473=
ENST00000367255.9:c.20634C>A	ENSP00000356224.5:p.Arg6878=
ENST00000367256.9:n.4326C>A
ENST00000409694.6:n.4218C>A
ENST00000423061.5:c.20421C>A	ENSP00000396024.1:p.Arg6807=
NM_033071.3:c.20421C>A	NP_149062.1:p.Arg6807=
NM_182961.3:c.20634C>A	NP_892006.3:p.Arg6878=
XM_006715407.1:c.20670C>A	XP_006715470.1:p.Arg6890=
XM_006715408.1:c.20658C>A	XP_006715471.1:p.Arg6886=
XM_006715409.1:c.20649C>A	XP_006715472.1:p.Arg6883=
XM_006715410.1:c.20670C>A	XP_006715473.1:p.Arg6890=
XM_006715411.1:c.20619C>A	XP_006715474.1:p.Arg6873=
XM_006715412.1:c.20655C>A	XP_006715475.1:p.Arg6885=
XM_006715413.1:c.20670C>A	XP_006715476.1:p.Arg6890=
XM_006715414.1:c.20598C>A	XP_006715477.1:p.Arg6866=
XM_006715415.1:c.20670C>A	XP_006715478.1:p.Arg6890=
XM_006715416.1:c.20655C>A	XP_006715479.1:p.Arg6885=
XM_006715417.1:c.20529C>A	XP_006715480.1:p.Arg6843=
XM_006715420.1:c.20517C>A	XP_006715483.1:p.Arg6839=
XM_006715421.1:c.20514C>A	XP_006715484.1:p.Arg6838=
XM_006715422.1:c.20511C>A	XP_006715485.1:p.Arg6837=
XM_006715423.1:c.20670C>A	XP_006715486.1:p.Arg6890=
XM_006715424.1:c.20670C>A	XP_006715487.1:p.Arg6890=
XM_006715425.1:c.20670C>A	XP_006715488.1:p.Arg6890=
XM_011535641.1:c.20667C>A	XP_011533943.1:p.Arg6889=
XM_011535642.1:c.20655C>A	XP_011533944.1:p.Arg6885=
XM_011535643.1:c.20505C>A	XP_011533945.1:p.Arg6835=
XM_011535644.1:c.18945C>A	XP_011533946.1:p.Arg6315=
XM_011535645.1:c.18438C>A	XP_011533947.1:p.Arg6146=
XM_011535647.1:c.13905C>A	XP_011533949.1:p.Arg4635=
XM_006715408.2:c.20658C>A	XP_006715471.1:p.Arg6886=
XM_006715410.2:c.20670C>A	XP_006715473.1:p.Arg6890=
XM_006715412.2:c.20655C>A	XP_006715475.1:p.Arg6885=
XM_006715413.2:c.20670C>A	XP_006715476.1:p.Arg6890=
XM_006715415.2:c.20670C>A	XP_006715478.1:p.Arg6890=
XM_006715416.2:c.20655C>A	XP_006715479.1:p.Arg6885=
XM_006715417.2:c.20529C>A	XP_006715480.1:p.Arg6843=
XM_006715420.2:c.20517C>A	XP_006715483.1:p.Arg6839=
XM_006715421.2:c.20514C>A	XP_006715484.1:p.Arg6838=
XM_006715423.2:c.20670C>A	XP_006715486.1:p.Arg6890=
XM_006715424.2:c.20670C>A	XP_006715487.1:p.Arg6890=
XM_006715425.2:c.20670C>A	XP_006715488.1:p.Arg6890=
XM_011535641.2:c.20667C>A	XP_011533943.1:p.Arg6889=
XM_011535642.2:c.20655C>A	XP_011533944.1:p.Arg6885=
XM_011535645.2:c.18438C>A	XP_011533947.1:p.Arg6146=
XM_017010608.1:c.20670C>A	XP_016866097.1:p.Arg6890=
XM_017010609.1:c.20670C>A	XP_016866098.1:p.Arg6890=
XM_017010610.1:c.20649C>A	XP_016866099.1:p.Arg6883=
XM_017010611.2:c.20643C>A	XP_016866100.1:p.Arg6881=
XM_017010612.1:c.20592C>A	XP_016866101.1:p.Arg6864=
XM_017010613.1:c.20667C>A	XP_016866102.1:p.Arg6889=
XM_017010614.1:c.20514C>A	XP_016866103.1:p.Arg6838=
XM_017010615.1:c.20514C>A	XP_016866104.1:p.Arg6838=
XM_017010616.1:c.20670C>A	XP_016866105.1:p.Arg6890=
XM_017010617.1:c.20667C>A	XP_016866106.1:p.Arg6889=
XM_017010618.1:c.20655C>A	XP_016866107.1:p.Arg6885=
XM_017010619.1:c.18945C>A	XP_016866108.1:p.Arg6315=
NM_182961.4:c.20634C>A MANE Select	NP_892006.3:p.Arg6878=
NM_033071.5:c.20421C>A	NP_149062.2:p.Arg6807=