Canonical Allele Identifier: CA10606486

Gene: SYNE1

Linked Data

• ClinVar Variation Id: 289576
• ClinVar RCV Id: RCV000364901 ; RCV002059267
• dbSNP Id: rs886044212
• gnomAD v4: 6-152254985-T-C
• MyVariant Identifiers: chr6:g.152576120T>C (hg19) ; chr6:g.152254985T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152254985T>C , CM000668.2:g.152254985T>C	GRCh38
NC_000006.11:g.152576120T>C , CM000668.1:g.152576120T>C	GRCh37
NC_000006.10:g.152617813T>C	NCBI36
NG_012855.1:g.387415A>G
NG_012855.2:g.387415A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.19365A>G MANE Select	ENSP00000356224.5:p.Glu6455=
ENST00000423061.6:c.19152A>G	ENSP00000396024.1:p.Glu6384=
ENST00000341594.9:c.18150A>G	ENSP00000341887.6:p.Glu6050=
ENST00000367255.9:c.19365A>G	ENSP00000356224.5:p.Glu6455=
ENST00000367256.9:n.3057A>G
ENST00000409694.6:n.2949A>G
ENST00000423061.5:c.19152A>G	ENSP00000396024.1:p.Glu6384=
NM_033071.3:c.19152A>G	NP_149062.1:p.Glu6384=
NM_182961.3:c.19365A>G	NP_892006.3:p.Glu6455=
XM_006715407.1:c.19401A>G	XP_006715470.1:p.Glu6467=
XM_006715408.1:c.19389A>G	XP_006715471.1:p.Glu6463=
XM_006715409.1:c.19380A>G	XP_006715472.1:p.Glu6460=
XM_006715410.1:c.19401A>G	XP_006715473.1:p.Glu6467=
XM_006715411.1:c.19350A>G	XP_006715474.1:p.Glu6450=
XM_006715412.1:c.19386A>G	XP_006715475.1:p.Glu6462=
XM_006715413.1:c.19401A>G	XP_006715476.1:p.Glu6467=
XM_006715414.1:c.19329A>G	XP_006715477.1:p.Glu6443=
XM_006715415.1:c.19401A>G	XP_006715478.1:p.Glu6467=
XM_006715416.1:c.19386A>G	XP_006715479.1:p.Glu6462=
XM_006715417.1:c.19260A>G	XP_006715480.1:p.Glu6420=
XM_006715420.1:c.19248A>G	XP_006715483.1:p.Glu6416=
XM_006715421.1:c.19245A>G	XP_006715484.1:p.Glu6415=
XM_006715422.1:c.19242A>G	XP_006715485.1:p.Glu6414=
XM_006715423.1:c.19401A>G	XP_006715486.1:p.Glu6467=
XM_006715424.1:c.19401A>G	XP_006715487.1:p.Glu6467=
XM_006715425.1:c.19401A>G	XP_006715488.1:p.Glu6467=
XM_011535641.1:c.19398A>G	XP_011533943.1:p.Glu6466=
XM_011535642.1:c.19386A>G	XP_011533944.1:p.Glu6462=
XM_011535643.1:c.19236A>G	XP_011533945.1:p.Glu6412=
XM_011535644.1:c.17676A>G	XP_011533946.1:p.Glu5892=
XM_011535645.1:c.17169A>G	XP_011533947.1:p.Glu5723=
XM_011535646.1:c.19401A>G	XP_011533948.1:p.Glu6467=
XM_011535647.1:c.12636A>G	XP_011533949.1:p.Glu4212=
XM_006715408.2:c.19389A>G	XP_006715471.1:p.Glu6463=
XM_006715410.2:c.19401A>G	XP_006715473.1:p.Glu6467=
XM_006715412.2:c.19386A>G	XP_006715475.1:p.Glu6462=
XM_006715413.2:c.19401A>G	XP_006715476.1:p.Glu6467=
XM_006715415.2:c.19401A>G	XP_006715478.1:p.Glu6467=
XM_006715416.2:c.19386A>G	XP_006715479.1:p.Glu6462=
XM_006715417.2:c.19260A>G	XP_006715480.1:p.Glu6420=
XM_006715420.2:c.19248A>G	XP_006715483.1:p.Glu6416=
XM_006715421.2:c.19245A>G	XP_006715484.1:p.Glu6415=
XM_006715423.2:c.19401A>G	XP_006715486.1:p.Glu6467=
XM_006715424.2:c.19401A>G	XP_006715487.1:p.Glu6467=
XM_006715425.2:c.19401A>G	XP_006715488.1:p.Glu6467=
XM_011535641.2:c.19398A>G	XP_011533943.1:p.Glu6466=
XM_011535642.2:c.19386A>G	XP_011533944.1:p.Glu6462=
XM_011535645.2:c.17169A>G	XP_011533947.1:p.Glu5723=
XM_017010608.1:c.19401A>G	XP_016866097.1:p.Glu6467=
XM_017010609.1:c.19401A>G	XP_016866098.1:p.Glu6467=
XM_017010610.1:c.19380A>G	XP_016866099.1:p.Glu6460=
XM_017010611.2:c.19374A>G	XP_016866100.1:p.Glu6458=
XM_017010612.1:c.19323A>G	XP_016866101.1:p.Glu6441=
XM_017010613.1:c.19398A>G	XP_016866102.1:p.Glu6466=
XM_017010614.1:c.19245A>G	XP_016866103.1:p.Glu6415=
XM_017010615.1:c.19245A>G	XP_016866104.1:p.Glu6415=
XM_017010616.1:c.19401A>G	XP_016866105.1:p.Glu6467=
XM_017010617.1:c.19398A>G	XP_016866106.1:p.Glu6466=
XM_017010618.1:c.19386A>G	XP_016866107.1:p.Glu6462=
XM_017010619.1:c.17676A>G	XP_016866108.1:p.Glu5892=
XR_001743287.1:n.19884A>G
NM_182961.4:c.19365A>G MANE Select	NP_892006.3:p.Glu6455=
NM_033071.5:c.19152A>G	NP_149062.2:p.Glu6384=