Canonical Allele Identifier: CA366099488

Gene: SYNE1

Linked Data

• ClinVar Variation Id: 2436582
• ClinVar RCV Id: RCV003138918
• MyVariant Identifiers: chr6:g.152534863T>C (hg19) ; chr6:g.152213728T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213728T>C , CM000668.2:g.152213728T>C	GRCh38
NC_000006.11:g.152534863T>C , CM000668.1:g.152534863T>C	GRCh37
NC_000006.10:g.152576556T>C	NCBI36
NG_012855.1:g.428672A>G
NG_012855.2:g.428672A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22378A>G MANE Select	ENSP00000356224.5:p.Thr7460Ala
ENST00000423061.6:c.22165A>G	ENSP00000396024.1:p.Thr7389Ala
ENST00000341594.9:c.21163A>G	ENSP00000341887.6:p.Thr7055Ala
ENST00000367251.7:c.1144A>G	ENSP00000356220.3:p.Thr382Ala
ENST00000367255.9:c.22378A>G	ENSP00000356224.5:p.Thr7460Ala
ENST00000367256.9:n.6070A>G
ENST00000367257.8:c.316A>G	ENSP00000356226.4:p.Thr106Ala
ENST00000409694.6:n.5962A>G
ENST00000423061.5:c.22165A>G	ENSP00000396024.1:p.Thr7389Ala
NM_033071.3:c.22165A>G	NP_149062.1:p.Thr7389Ala
NM_182961.3:c.22378A>G	NP_892006.3:p.Thr7460Ala
XM_006715407.1:c.22414A>G	XP_006715470.1:p.Thr7472Ala
XM_006715408.1:c.22402A>G	XP_006715471.1:p.Thr7468Ala
XM_006715409.1:c.22393A>G	XP_006715472.1:p.Thr7465Ala
XM_006715410.1:c.22414A>G	XP_006715473.1:p.Thr7472Ala
XM_006715411.1:c.22363A>G	XP_006715474.1:p.Thr7455Ala
XM_006715412.1:c.22399A>G	XP_006715475.1:p.Thr7467Ala
XM_006715413.1:c.22414A>G	XP_006715476.1:p.Thr7472Ala
XM_006715414.1:c.22342A>G	XP_006715477.1:p.Thr7448Ala
XM_006715415.1:c.22414A>G	XP_006715478.1:p.Thr7472Ala
XM_006715416.1:c.22399A>G	XP_006715479.1:p.Thr7467Ala
XM_006715417.1:c.22273A>G	XP_006715480.1:p.Thr7425Ala
XM_006715420.1:c.22261A>G	XP_006715483.1:p.Thr7421Ala
XM_006715421.1:c.22258A>G	XP_006715484.1:p.Thr7420Ala
XM_006715422.1:c.22255A>G	XP_006715485.1:p.Thr7419Ala
XM_006715423.1:c.22414A>G	XP_006715486.1:p.Thr7472Ala
XM_006715424.1:c.22414A>G	XP_006715487.1:p.Thr7472Ala
XM_006715425.1:c.22414A>G	XP_006715488.1:p.Thr7472Ala
XM_011535641.1:c.22411A>G	XP_011533943.1:p.Thr7471Ala
XM_011535642.1:c.22399A>G	XP_011533944.1:p.Thr7467Ala
XM_011535643.1:c.22249A>G	XP_011533945.1:p.Thr7417Ala
XM_011535644.1:c.20689A>G	XP_011533946.1:p.Thr6897Ala
XM_011535645.1:c.20182A>G	XP_011533947.1:p.Thr6728Ala
XM_011535647.1:c.15649A>G	XP_011533949.1:p.Thr5217Ala
XM_006715408.2:c.22402A>G	XP_006715471.1:p.Thr7468Ala
XM_006715410.2:c.22414A>G	XP_006715473.1:p.Thr7472Ala
XM_006715412.2:c.22399A>G	XP_006715475.1:p.Thr7467Ala
XM_006715413.2:c.22414A>G	XP_006715476.1:p.Thr7472Ala
XM_006715415.2:c.22414A>G	XP_006715478.1:p.Thr7472Ala
XM_006715416.2:c.22399A>G	XP_006715479.1:p.Thr7467Ala
XM_006715417.2:c.22273A>G	XP_006715480.1:p.Thr7425Ala
XM_006715420.2:c.22261A>G	XP_006715483.1:p.Thr7421Ala
XM_006715421.2:c.22258A>G	XP_006715484.1:p.Thr7420Ala
XM_006715423.2:c.22414A>G	XP_006715486.1:p.Thr7472Ala
XM_006715424.2:c.22414A>G	XP_006715487.1:p.Thr7472Ala
XM_006715425.2:c.22414A>G	XP_006715488.1:p.Thr7472Ala
XM_011535641.2:c.22411A>G	XP_011533943.1:p.Thr7471Ala
XM_011535642.2:c.22399A>G	XP_011533944.1:p.Thr7467Ala
XM_011535645.2:c.20182A>G	XP_011533947.1:p.Thr6728Ala
XM_017010608.1:c.22414A>G	XP_016866097.1:p.Thr7472Ala
XM_017010609.1:c.22414A>G	XP_016866098.1:p.Thr7472Ala
XM_017010610.1:c.22393A>G	XP_016866099.1:p.Thr7465Ala
XM_017010611.2:c.22387A>G	XP_016866100.1:p.Thr7463Ala
XM_017010612.1:c.22336A>G	XP_016866101.1:p.Thr7446Ala
XM_017010613.1:c.22411A>G	XP_016866102.1:p.Thr7471Ala
XM_017010614.1:c.22258A>G	XP_016866103.1:p.Thr7420Ala
XM_017010615.1:c.22258A>G	XP_016866104.1:p.Thr7420Ala
XM_017010616.1:c.22414A>G	XP_016866105.1:p.Thr7472Ala
XM_017010617.1:c.22411A>G	XP_016866106.1:p.Thr7471Ala
XM_017010618.1:c.22399A>G	XP_016866107.1:p.Thr7467Ala
XM_017010619.1:c.20689A>G	XP_016866108.1:p.Thr6897Ala
NM_182961.4:c.22378A>G MANE Select	NP_892006.3:p.Thr7460Ala
NM_033071.5:c.22165A>G	NP_149062.2:p.Thr7389Ala