Canonical Allele Identifier: CA366099204

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534802G>A (hg19) ; chr6:g.152213667G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213667G>A , CM000668.2:g.152213667G>A	GRCh38
NC_000006.11:g.152534802G>A , CM000668.1:g.152534802G>A	GRCh37
NC_000006.10:g.152576495G>A	NCBI36
NG_012855.1:g.428733C>T
NG_012855.2:g.428733C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22439C>T MANE Select	ENSP00000356224.5:p.Ala7480Val
ENST00000423061.6:c.22226C>T	ENSP00000396024.1:p.Ala7409Val
ENST00000341594.9:c.21224C>T	ENSP00000341887.6:p.Ala7075Val
ENST00000367251.7:c.1205C>T	ENSP00000356220.3:p.Ala402Val
ENST00000367255.9:c.22439C>T	ENSP00000356224.5:p.Ala7480Val
ENST00000367256.9:n.6131C>T
ENST00000367257.8:c.377C>T	ENSP00000356226.4:p.Ala126Val
ENST00000409694.6:n.6023C>T
ENST00000423061.5:c.22226C>T	ENSP00000396024.1:p.Ala7409Val
NM_033071.3:c.22226C>T	NP_149062.1:p.Ala7409Val
NM_182961.3:c.22439C>T	NP_892006.3:p.Ala7480Val
XM_006715407.1:c.22475C>T	XP_006715470.1:p.Ala7492Val
XM_006715408.1:c.22463C>T	XP_006715471.1:p.Ala7488Val
XM_006715409.1:c.22454C>T	XP_006715472.1:p.Ala7485Val
XM_006715410.1:c.22475C>T	XP_006715473.1:p.Ala7492Val
XM_006715411.1:c.22424C>T	XP_006715474.1:p.Ala7475Val
XM_006715412.1:c.22460C>T	XP_006715475.1:p.Ala7487Val
XM_006715413.1:c.22475C>T	XP_006715476.1:p.Ala7492Val
XM_006715414.1:c.22403C>T	XP_006715477.1:p.Ala7468Val
XM_006715415.1:c.22475C>T	XP_006715478.1:p.Ala7492Val
XM_006715416.1:c.22460C>T	XP_006715479.1:p.Ala7487Val
XM_006715417.1:c.22334C>T	XP_006715480.1:p.Ala7445Val
XM_006715420.1:c.22322C>T	XP_006715483.1:p.Ala7441Val
XM_006715421.1:c.22319C>T	XP_006715484.1:p.Ala7440Val
XM_006715422.1:c.22316C>T	XP_006715485.1:p.Ala7439Val
XM_006715423.1:c.22475C>T	XP_006715486.1:p.Ala7492Val
XM_006715424.1:c.22475C>T	XP_006715487.1:p.Ala7492Val
XM_006715425.1:c.22475C>T	XP_006715488.1:p.Ala7492Val
XM_011535641.1:c.22472C>T	XP_011533943.1:p.Ala7491Val
XM_011535642.1:c.22460C>T	XP_011533944.1:p.Ala7487Val
XM_011535643.1:c.22310C>T	XP_011533945.1:p.Ala7437Val
XM_011535644.1:c.20750C>T	XP_011533946.1:p.Ala6917Val
XM_011535645.1:c.20243C>T	XP_011533947.1:p.Ala6748Val
XM_011535647.1:c.15710C>T	XP_011533949.1:p.Ala5237Val
XM_006715408.2:c.22463C>T	XP_006715471.1:p.Ala7488Val
XM_006715410.2:c.22475C>T	XP_006715473.1:p.Ala7492Val
XM_006715412.2:c.22460C>T	XP_006715475.1:p.Ala7487Val
XM_006715413.2:c.22475C>T	XP_006715476.1:p.Ala7492Val
XM_006715415.2:c.22475C>T	XP_006715478.1:p.Ala7492Val
XM_006715416.2:c.22460C>T	XP_006715479.1:p.Ala7487Val
XM_006715417.2:c.22334C>T	XP_006715480.1:p.Ala7445Val
XM_006715420.2:c.22322C>T	XP_006715483.1:p.Ala7441Val
XM_006715421.2:c.22319C>T	XP_006715484.1:p.Ala7440Val
XM_006715423.2:c.22475C>T	XP_006715486.1:p.Ala7492Val
XM_006715424.2:c.22475C>T	XP_006715487.1:p.Ala7492Val
XM_006715425.2:c.22475C>T	XP_006715488.1:p.Ala7492Val
XM_011535641.2:c.22472C>T	XP_011533943.1:p.Ala7491Val
XM_011535642.2:c.22460C>T	XP_011533944.1:p.Ala7487Val
XM_011535645.2:c.20243C>T	XP_011533947.1:p.Ala6748Val
XM_017010608.1:c.22475C>T	XP_016866097.1:p.Ala7492Val
XM_017010609.1:c.22475C>T	XP_016866098.1:p.Ala7492Val
XM_017010610.1:c.22454C>T	XP_016866099.1:p.Ala7485Val
XM_017010611.2:c.22448C>T	XP_016866100.1:p.Ala7483Val
XM_017010612.1:c.22397C>T	XP_016866101.1:p.Ala7466Val
XM_017010613.1:c.22472C>T	XP_016866102.1:p.Ala7491Val
XM_017010614.1:c.22319C>T	XP_016866103.1:p.Ala7440Val
XM_017010615.1:c.22319C>T	XP_016866104.1:p.Ala7440Val
XM_017010616.1:c.22475C>T	XP_016866105.1:p.Ala7492Val
XM_017010617.1:c.22472C>T	XP_016866106.1:p.Ala7491Val
XM_017010618.1:c.22460C>T	XP_016866107.1:p.Ala7487Val
XM_017010619.1:c.20750C>T	XP_016866108.1:p.Ala6917Val
NM_182961.4:c.22439C>T MANE Select	NP_892006.3:p.Ala7480Val
NM_033071.5:c.22226C>T	NP_149062.2:p.Ala7409Val