Canonical Allele Identifier: CA4054535

Gene: SYNE1

Linked Data

• ClinVar Variation Id: 290531
• ClinVar RCV Id: RCV000276438 ; RCV001155835 ; RCV001155836 ; RCV001859719
• dbSNP Id: rs376891338
• ExAC: 6:152560763 T / C
• gnomAD v2: 6-152560763-T-C
• gnomAD v3: 6-152239628-T-C
• gnomAD v4: 6-152239628-T-C
• MyVariant Identifiers: chr6:g.152560763T>C (hg19) ; chr6:g.152239628T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152239628T>C , CM000668.2:g.152239628T>C	GRCh38
NC_000006.11:g.152560763T>C , CM000668.1:g.152560763T>C	GRCh37
NC_000006.10:g.152602456T>C	NCBI36
NG_012855.1:g.402772A>G
NG_012855.2:g.402772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.19972A>G MANE Select	ENSP00000356224.5:p.Lys6658Glu
ENST00000423061.6:c.19759A>G	ENSP00000396024.1:p.Lys6587Glu
ENST00000341594.9:c.18757A>G	ENSP00000341887.6:p.Lys6253Glu
ENST00000367255.9:c.19972A>G	ENSP00000356224.5:p.Lys6658Glu
ENST00000367256.9:n.3664A>G
ENST00000409694.6:n.3556A>G
ENST00000423061.5:c.19759A>G	ENSP00000396024.1:p.Lys6587Glu
NM_033071.3:c.19759A>G	NP_149062.1:p.Lys6587Glu
NM_182961.3:c.19972A>G	NP_892006.3:p.Lys6658Glu
XM_006715407.1:c.20008A>G	XP_006715470.1:p.Lys6670Glu
XM_006715408.1:c.19996A>G	XP_006715471.1:p.Lys6666Glu
XM_006715409.1:c.19987A>G	XP_006715472.1:p.Lys6663Glu
XM_006715410.1:c.20008A>G	XP_006715473.1:p.Lys6670Glu
XM_006715411.1:c.19957A>G	XP_006715474.1:p.Lys6653Glu
XM_006715412.1:c.19993A>G	XP_006715475.1:p.Lys6665Glu
XM_006715413.1:c.20008A>G	XP_006715476.1:p.Lys6670Glu
XM_006715414.1:c.19936A>G	XP_006715477.1:p.Lys6646Glu
XM_006715415.1:c.20008A>G	XP_006715478.1:p.Lys6670Glu
XM_006715416.1:c.19993A>G	XP_006715479.1:p.Lys6665Glu
XM_006715417.1:c.19867A>G	XP_006715480.1:p.Lys6623Glu
XM_006715420.1:c.19855A>G	XP_006715483.1:p.Lys6619Glu
XM_006715421.1:c.19852A>G	XP_006715484.1:p.Lys6618Glu
XM_006715422.1:c.19849A>G	XP_006715485.1:p.Lys6617Glu
XM_006715423.1:c.20008A>G	XP_006715486.1:p.Lys6670Glu
XM_006715424.1:c.20008A>G	XP_006715487.1:p.Lys6670Glu
XM_006715425.1:c.20008A>G	XP_006715488.1:p.Lys6670Glu
XM_011535641.1:c.20005A>G	XP_011533943.1:p.Lys6669Glu
XM_011535642.1:c.19993A>G	XP_011533944.1:p.Lys6665Glu
XM_011535643.1:c.19843A>G	XP_011533945.1:p.Lys6615Glu
XM_011535644.1:c.18283A>G	XP_011533946.1:p.Lys6095Glu
XM_011535645.1:c.17776A>G	XP_011533947.1:p.Lys5926Glu
XM_011535647.1:c.13243A>G	XP_011533949.1:p.Lys4415Glu
XM_006715408.2:c.19996A>G	XP_006715471.1:p.Lys6666Glu
XM_006715410.2:c.20008A>G	XP_006715473.1:p.Lys6670Glu
XM_006715412.2:c.19993A>G	XP_006715475.1:p.Lys6665Glu
XM_006715413.2:c.20008A>G	XP_006715476.1:p.Lys6670Glu
XM_006715415.2:c.20008A>G	XP_006715478.1:p.Lys6670Glu
XM_006715416.2:c.19993A>G	XP_006715479.1:p.Lys6665Glu
XM_006715417.2:c.19867A>G	XP_006715480.1:p.Lys6623Glu
XM_006715420.2:c.19855A>G	XP_006715483.1:p.Lys6619Glu
XM_006715421.2:c.19852A>G	XP_006715484.1:p.Lys6618Glu
XM_006715423.2:c.20008A>G	XP_006715486.1:p.Lys6670Glu
XM_006715424.2:c.20008A>G	XP_006715487.1:p.Lys6670Glu
XM_006715425.2:c.20008A>G	XP_006715488.1:p.Lys6670Glu
XM_011535641.2:c.20005A>G	XP_011533943.1:p.Lys6669Glu
XM_011535642.2:c.19993A>G	XP_011533944.1:p.Lys6665Glu
XM_011535645.2:c.17776A>G	XP_011533947.1:p.Lys5926Glu
XM_017010608.1:c.20008A>G	XP_016866097.1:p.Lys6670Glu
XM_017010609.1:c.20008A>G	XP_016866098.1:p.Lys6670Glu
XM_017010610.1:c.19987A>G	XP_016866099.1:p.Lys6663Glu
XM_017010611.2:c.19981A>G	XP_016866100.1:p.Lys6661Glu
XM_017010612.1:c.19930A>G	XP_016866101.1:p.Lys6644Glu
XM_017010613.1:c.20005A>G	XP_016866102.1:p.Lys6669Glu
XM_017010614.1:c.19852A>G	XP_016866103.1:p.Lys6618Glu
XM_017010615.1:c.19852A>G	XP_016866104.1:p.Lys6618Glu
XM_017010616.1:c.20008A>G	XP_016866105.1:p.Lys6670Glu
XM_017010617.1:c.20005A>G	XP_016866106.1:p.Lys6669Glu
XM_017010618.1:c.19993A>G	XP_016866107.1:p.Lys6665Glu
XM_017010619.1:c.18283A>G	XP_016866108.1:p.Lys6095Glu
NM_182961.4:c.19972A>G MANE Select	NP_892006.3:p.Lys6658Glu
NM_033071.5:c.19759A>G	NP_149062.2:p.Lys6587Glu