Canonical Allele Identifier: CA366099379

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534841G>C (hg19) ; chr6:g.152213706G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213706G>C , CM000668.2:g.152213706G>C	GRCh38
NC_000006.11:g.152534841G>C , CM000668.1:g.152534841G>C	GRCh37
NC_000006.10:g.152576534G>C	NCBI36
NG_012855.1:g.428694C>G
NG_012855.2:g.428694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22400C>G MANE Select	ENSP00000356224.5:p.Thr7467Arg
ENST00000423061.6:c.22187C>G	ENSP00000396024.1:p.Thr7396Arg
ENST00000341594.9:c.21185C>G	ENSP00000341887.6:p.Thr7062Arg
ENST00000367251.7:c.1166C>G	ENSP00000356220.3:p.Thr389Arg
ENST00000367255.9:c.22400C>G	ENSP00000356224.5:p.Thr7467Arg
ENST00000367256.9:n.6092C>G
ENST00000367257.8:c.338C>G	ENSP00000356226.4:p.Thr113Arg
ENST00000409694.6:n.5984C>G
ENST00000423061.5:c.22187C>G	ENSP00000396024.1:p.Thr7396Arg
NM_033071.3:c.22187C>G	NP_149062.1:p.Thr7396Arg
NM_182961.3:c.22400C>G	NP_892006.3:p.Thr7467Arg
XM_006715407.1:c.22436C>G	XP_006715470.1:p.Thr7479Arg
XM_006715408.1:c.22424C>G	XP_006715471.1:p.Thr7475Arg
XM_006715409.1:c.22415C>G	XP_006715472.1:p.Thr7472Arg
XM_006715410.1:c.22436C>G	XP_006715473.1:p.Thr7479Arg
XM_006715411.1:c.22385C>G	XP_006715474.1:p.Thr7462Arg
XM_006715412.1:c.22421C>G	XP_006715475.1:p.Thr7474Arg
XM_006715413.1:c.22436C>G	XP_006715476.1:p.Thr7479Arg
XM_006715414.1:c.22364C>G	XP_006715477.1:p.Thr7455Arg
XM_006715415.1:c.22436C>G	XP_006715478.1:p.Thr7479Arg
XM_006715416.1:c.22421C>G	XP_006715479.1:p.Thr7474Arg
XM_006715417.1:c.22295C>G	XP_006715480.1:p.Thr7432Arg
XM_006715420.1:c.22283C>G	XP_006715483.1:p.Thr7428Arg
XM_006715421.1:c.22280C>G	XP_006715484.1:p.Thr7427Arg
XM_006715422.1:c.22277C>G	XP_006715485.1:p.Thr7426Arg
XM_006715423.1:c.22436C>G	XP_006715486.1:p.Thr7479Arg
XM_006715424.1:c.22436C>G	XP_006715487.1:p.Thr7479Arg
XM_006715425.1:c.22436C>G	XP_006715488.1:p.Thr7479Arg
XM_011535641.1:c.22433C>G	XP_011533943.1:p.Thr7478Arg
XM_011535642.1:c.22421C>G	XP_011533944.1:p.Thr7474Arg
XM_011535643.1:c.22271C>G	XP_011533945.1:p.Thr7424Arg
XM_011535644.1:c.20711C>G	XP_011533946.1:p.Thr6904Arg
XM_011535645.1:c.20204C>G	XP_011533947.1:p.Thr6735Arg
XM_011535647.1:c.15671C>G	XP_011533949.1:p.Thr5224Arg
XM_006715408.2:c.22424C>G	XP_006715471.1:p.Thr7475Arg
XM_006715410.2:c.22436C>G	XP_006715473.1:p.Thr7479Arg
XM_006715412.2:c.22421C>G	XP_006715475.1:p.Thr7474Arg
XM_006715413.2:c.22436C>G	XP_006715476.1:p.Thr7479Arg
XM_006715415.2:c.22436C>G	XP_006715478.1:p.Thr7479Arg
XM_006715416.2:c.22421C>G	XP_006715479.1:p.Thr7474Arg
XM_006715417.2:c.22295C>G	XP_006715480.1:p.Thr7432Arg
XM_006715420.2:c.22283C>G	XP_006715483.1:p.Thr7428Arg
XM_006715421.2:c.22280C>G	XP_006715484.1:p.Thr7427Arg
XM_006715423.2:c.22436C>G	XP_006715486.1:p.Thr7479Arg
XM_006715424.2:c.22436C>G	XP_006715487.1:p.Thr7479Arg
XM_006715425.2:c.22436C>G	XP_006715488.1:p.Thr7479Arg
XM_011535641.2:c.22433C>G	XP_011533943.1:p.Thr7478Arg
XM_011535642.2:c.22421C>G	XP_011533944.1:p.Thr7474Arg
XM_011535645.2:c.20204C>G	XP_011533947.1:p.Thr6735Arg
XM_017010608.1:c.22436C>G	XP_016866097.1:p.Thr7479Arg
XM_017010609.1:c.22436C>G	XP_016866098.1:p.Thr7479Arg
XM_017010610.1:c.22415C>G	XP_016866099.1:p.Thr7472Arg
XM_017010611.2:c.22409C>G	XP_016866100.1:p.Thr7470Arg
XM_017010612.1:c.22358C>G	XP_016866101.1:p.Thr7453Arg
XM_017010613.1:c.22433C>G	XP_016866102.1:p.Thr7478Arg
XM_017010614.1:c.22280C>G	XP_016866103.1:p.Thr7427Arg
XM_017010615.1:c.22280C>G	XP_016866104.1:p.Thr7427Arg
XM_017010616.1:c.22436C>G	XP_016866105.1:p.Thr7479Arg
XM_017010617.1:c.22433C>G	XP_016866106.1:p.Thr7478Arg
XM_017010618.1:c.22421C>G	XP_016866107.1:p.Thr7474Arg
XM_017010619.1:c.20711C>G	XP_016866108.1:p.Thr6904Arg
NM_182961.4:c.22400C>G MANE Select	NP_892006.3:p.Thr7467Arg
NM_033071.5:c.22187C>G	NP_149062.2:p.Thr7396Arg