Canonical Allele Identifier: CA4055990

Gene: SYNE1

Linked Data

• ClinVar Variation Id: 355870
• ClinVar RCV Id: RCV000269205 ; RCV000326527 ; RCV001288819 ; RCV001211385
• dbSNP Id: rs747838657
• ExAC: 6:152651290 G / T
• gnomAD v2: 6-152651290-G-T
• gnomAD v3: 6-152330155-G-T
• gnomAD v4: 6-152330155-G-T
• MyVariant Identifiers: chr6:g.152651290G>T (hg19) ; chr6:g.152330155G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152330155G>T , CM000668.2:g.152330155G>T	GRCh38
NC_000006.11:g.152651290G>T , CM000668.1:g.152651290G>T	GRCh37
NC_000006.10:g.152692983G>T	NCBI36
NG_012855.1:g.312245C>A
NG_012855.2:g.312245C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.14530C>A MANE Select	ENSP00000356224.5:p.Pro4844Thr
ENST00000423061.6:c.14317C>A	ENSP00000396024.1:p.Pro4773Thr
ENST00000341594.9:c.13720C>A	ENSP00000341887.6:p.Pro4574Thr
ENST00000367255.9:c.14530C>A	ENSP00000356224.5:p.Pro4844Thr
ENST00000423061.5:c.14317C>A	ENSP00000396024.1:p.Pro4773Thr
ENST00000448038.2:c.-1389C>A	ENSP00000390975.2:n.-1389C>A
ENST00000490135.6:n.1876C>A
NM_033071.3:c.14317C>A	NP_149062.1:p.Pro4773Thr
NM_182961.3:c.14530C>A	NP_892006.3:p.Pro4844Thr
XM_006715407.1:c.14551C>A	XP_006715470.1:p.Pro4851Thr
XM_006715408.1:c.14551C>A	XP_006715471.1:p.Pro4851Thr
XM_006715409.1:c.14530C>A	XP_006715472.1:p.Pro4844Thr
XM_006715410.1:c.14551C>A	XP_006715473.1:p.Pro4851Thr
XM_006715411.1:c.14500C>A	XP_006715474.1:p.Pro4834Thr
XM_006715412.1:c.14551C>A	XP_006715475.1:p.Pro4851Thr
XM_006715413.1:c.14551C>A	XP_006715476.1:p.Pro4851Thr
XM_006715414.1:c.14479C>A	XP_006715477.1:p.Pro4827Thr
XM_006715415.1:c.14551C>A	XP_006715478.1:p.Pro4851Thr
XM_006715416.1:c.14551C>A	XP_006715479.1:p.Pro4851Thr
XM_006715417.1:c.14551C>A	XP_006715480.1:p.Pro4851Thr
XM_006715420.1:c.14551C>A	XP_006715483.1:p.Pro4851Thr
XM_006715421.1:c.14395C>A	XP_006715484.1:p.Pro4799Thr
XM_006715422.1:c.14392C>A	XP_006715485.1:p.Pro4798Thr
XM_006715423.1:c.14551C>A	XP_006715486.1:p.Pro4851Thr
XM_006715424.1:c.14551C>A	XP_006715487.1:p.Pro4851Thr
XM_006715425.1:c.14551C>A	XP_006715488.1:p.Pro4851Thr
XM_011535641.1:c.14551C>A	XP_011533943.1:p.Pro4851Thr
XM_011535642.1:c.14551C>A	XP_011533944.1:p.Pro4851Thr
XM_011535643.1:c.14386C>A	XP_011533945.1:p.Pro4796Thr
XM_011535644.1:c.12826C>A	XP_011533946.1:p.Pro4276Thr
XM_011535645.1:c.12319C>A	XP_011533947.1:p.Pro4107Thr
XM_011535646.1:c.14551C>A	XP_011533948.1:p.Pro4851Thr
XM_011535647.1:c.7786C>A	XP_011533949.1:p.Pro2596Thr
XM_006715408.2:c.14551C>A	XP_006715471.1:p.Pro4851Thr
XM_006715410.2:c.14551C>A	XP_006715473.1:p.Pro4851Thr
XM_006715412.2:c.14551C>A	XP_006715475.1:p.Pro4851Thr
XM_006715413.2:c.14551C>A	XP_006715476.1:p.Pro4851Thr
XM_006715415.2:c.14551C>A	XP_006715478.1:p.Pro4851Thr
XM_006715416.2:c.14551C>A	XP_006715479.1:p.Pro4851Thr
XM_006715417.2:c.14551C>A	XP_006715480.1:p.Pro4851Thr
XM_006715420.2:c.14551C>A	XP_006715483.1:p.Pro4851Thr
XM_006715421.2:c.14395C>A	XP_006715484.1:p.Pro4799Thr
XM_006715423.2:c.14551C>A	XP_006715486.1:p.Pro4851Thr
XM_006715424.2:c.14551C>A	XP_006715487.1:p.Pro4851Thr
XM_006715425.2:c.14551C>A	XP_006715488.1:p.Pro4851Thr
XM_011535641.2:c.14551C>A	XP_011533943.1:p.Pro4851Thr
XM_011535642.2:c.14551C>A	XP_011533944.1:p.Pro4851Thr
XM_011535645.2:c.12319C>A	XP_011533947.1:p.Pro4107Thr
XM_017010608.1:c.14551C>A	XP_016866097.1:p.Pro4851Thr
XM_017010609.1:c.14551C>A	XP_016866098.1:p.Pro4851Thr
XM_017010610.1:c.14530C>A	XP_016866099.1:p.Pro4844Thr
XM_017010611.2:c.14524C>A	XP_016866100.1:p.Pro4842Thr
XM_017010612.1:c.14473C>A	XP_016866101.1:p.Pro4825Thr
XM_017010613.1:c.14551C>A	XP_016866102.1:p.Pro4851Thr
XM_017010614.1:c.14551C>A	XP_016866103.1:p.Pro4851Thr
XM_017010615.1:c.14551C>A	XP_016866104.1:p.Pro4851Thr
XM_017010616.1:c.14551C>A	XP_016866105.1:p.Pro4851Thr
XM_017010617.1:c.14551C>A	XP_016866106.1:p.Pro4851Thr
XM_017010618.1:c.14551C>A	XP_016866107.1:p.Pro4851Thr
XM_017010619.1:c.12826C>A	XP_016866108.1:p.Pro4276Thr
XR_001743287.1:n.15034C>A
NM_182961.4:c.14530C>A MANE Select	NP_892006.3:p.Pro4844Thr
NM_033071.5:c.14317C>A	NP_149062.2:p.Pro4773Thr