Canonical Allele Identifier: CA366099325

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534829A>G (hg19) ; chr6:g.152213694A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213694A>G , CM000668.2:g.152213694A>G	GRCh38
NC_000006.11:g.152534829A>G , CM000668.1:g.152534829A>G	GRCh37
NC_000006.10:g.152576522A>G	NCBI36
NG_012855.1:g.428706T>C
NG_012855.2:g.428706T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22412T>C MANE Select	ENSP00000356224.5:p.Phe7471Ser
ENST00000423061.6:c.22199T>C	ENSP00000396024.1:p.Phe7400Ser
ENST00000341594.9:c.21197T>C	ENSP00000341887.6:p.Phe7066Ser
ENST00000367251.7:c.1178T>C	ENSP00000356220.3:p.Phe393Ser
ENST00000367255.9:c.22412T>C	ENSP00000356224.5:p.Phe7471Ser
ENST00000367256.9:n.6104T>C
ENST00000367257.8:c.350T>C	ENSP00000356226.4:p.Phe117Ser
ENST00000409694.6:n.5996T>C
ENST00000423061.5:c.22199T>C	ENSP00000396024.1:p.Phe7400Ser
NM_033071.3:c.22199T>C	NP_149062.1:p.Phe7400Ser
NM_182961.3:c.22412T>C	NP_892006.3:p.Phe7471Ser
XM_006715407.1:c.22448T>C	XP_006715470.1:p.Phe7483Ser
XM_006715408.1:c.22436T>C	XP_006715471.1:p.Phe7479Ser
XM_006715409.1:c.22427T>C	XP_006715472.1:p.Phe7476Ser
XM_006715410.1:c.22448T>C	XP_006715473.1:p.Phe7483Ser
XM_006715411.1:c.22397T>C	XP_006715474.1:p.Phe7466Ser
XM_006715412.1:c.22433T>C	XP_006715475.1:p.Phe7478Ser
XM_006715413.1:c.22448T>C	XP_006715476.1:p.Phe7483Ser
XM_006715414.1:c.22376T>C	XP_006715477.1:p.Phe7459Ser
XM_006715415.1:c.22448T>C	XP_006715478.1:p.Phe7483Ser
XM_006715416.1:c.22433T>C	XP_006715479.1:p.Phe7478Ser
XM_006715417.1:c.22307T>C	XP_006715480.1:p.Phe7436Ser
XM_006715420.1:c.22295T>C	XP_006715483.1:p.Phe7432Ser
XM_006715421.1:c.22292T>C	XP_006715484.1:p.Phe7431Ser
XM_006715422.1:c.22289T>C	XP_006715485.1:p.Phe7430Ser
XM_006715423.1:c.22448T>C	XP_006715486.1:p.Phe7483Ser
XM_006715424.1:c.22448T>C	XP_006715487.1:p.Phe7483Ser
XM_006715425.1:c.22448T>C	XP_006715488.1:p.Phe7483Ser
XM_011535641.1:c.22445T>C	XP_011533943.1:p.Phe7482Ser
XM_011535642.1:c.22433T>C	XP_011533944.1:p.Phe7478Ser
XM_011535643.1:c.22283T>C	XP_011533945.1:p.Phe7428Ser
XM_011535644.1:c.20723T>C	XP_011533946.1:p.Phe6908Ser
XM_011535645.1:c.20216T>C	XP_011533947.1:p.Phe6739Ser
XM_011535647.1:c.15683T>C	XP_011533949.1:p.Phe5228Ser
XM_006715408.2:c.22436T>C	XP_006715471.1:p.Phe7479Ser
XM_006715410.2:c.22448T>C	XP_006715473.1:p.Phe7483Ser
XM_006715412.2:c.22433T>C	XP_006715475.1:p.Phe7478Ser
XM_006715413.2:c.22448T>C	XP_006715476.1:p.Phe7483Ser
XM_006715415.2:c.22448T>C	XP_006715478.1:p.Phe7483Ser
XM_006715416.2:c.22433T>C	XP_006715479.1:p.Phe7478Ser
XM_006715417.2:c.22307T>C	XP_006715480.1:p.Phe7436Ser
XM_006715420.2:c.22295T>C	XP_006715483.1:p.Phe7432Ser
XM_006715421.2:c.22292T>C	XP_006715484.1:p.Phe7431Ser
XM_006715423.2:c.22448T>C	XP_006715486.1:p.Phe7483Ser
XM_006715424.2:c.22448T>C	XP_006715487.1:p.Phe7483Ser
XM_006715425.2:c.22448T>C	XP_006715488.1:p.Phe7483Ser
XM_011535641.2:c.22445T>C	XP_011533943.1:p.Phe7482Ser
XM_011535642.2:c.22433T>C	XP_011533944.1:p.Phe7478Ser
XM_011535645.2:c.20216T>C	XP_011533947.1:p.Phe6739Ser
XM_017010608.1:c.22448T>C	XP_016866097.1:p.Phe7483Ser
XM_017010609.1:c.22448T>C	XP_016866098.1:p.Phe7483Ser
XM_017010610.1:c.22427T>C	XP_016866099.1:p.Phe7476Ser
XM_017010611.2:c.22421T>C	XP_016866100.1:p.Phe7474Ser
XM_017010612.1:c.22370T>C	XP_016866101.1:p.Phe7457Ser
XM_017010613.1:c.22445T>C	XP_016866102.1:p.Phe7482Ser
XM_017010614.1:c.22292T>C	XP_016866103.1:p.Phe7431Ser
XM_017010615.1:c.22292T>C	XP_016866104.1:p.Phe7431Ser
XM_017010616.1:c.22448T>C	XP_016866105.1:p.Phe7483Ser
XM_017010617.1:c.22445T>C	XP_016866106.1:p.Phe7482Ser
XM_017010618.1:c.22433T>C	XP_016866107.1:p.Phe7478Ser
XM_017010619.1:c.20723T>C	XP_016866108.1:p.Phe6908Ser
NM_182961.4:c.22412T>C MANE Select	NP_892006.3:p.Phe7471Ser
NM_033071.5:c.22199T>C	NP_149062.2:p.Phe7400Ser