Canonical Allele Identifier: CA452748457

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534816T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213681T>A , CM000668.2:g.152213681T>A	GRCh38
NC_000006.11:g.152534816T>A , CM000668.1:g.152534816T>A	GRCh37
NC_000006.10:g.152576509T>A	NCBI36
NG_012855.1:g.428719A>T
NG_012855.2:g.428719A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22425A>T MANE Select	ENSP00000356224.5:p.Thr7475=
ENST00000423061.6:c.22212A>T	ENSP00000396024.1:p.Thr7404=
ENST00000341594.9:c.21210A>T	ENSP00000341887.6:p.Thr7070=
ENST00000367251.7:c.1191A>T	ENSP00000356220.3:p.Thr397=
ENST00000367255.9:c.22425A>T	ENSP00000356224.5:p.Thr7475=
ENST00000367256.9:n.6117A>T
ENST00000367257.8:c.363A>T	ENSP00000356226.4:p.Thr121=
ENST00000409694.6:n.6009A>T
ENST00000423061.5:c.22212A>T	ENSP00000396024.1:p.Thr7404=
NM_033071.3:c.22212A>T	NP_149062.1:p.Thr7404=
NM_182961.3:c.22425A>T	NP_892006.3:p.Thr7475=
XM_006715407.1:c.22461A>T	XP_006715470.1:p.Thr7487=
XM_006715408.1:c.22449A>T	XP_006715471.1:p.Thr7483=
XM_006715409.1:c.22440A>T	XP_006715472.1:p.Thr7480=
XM_006715410.1:c.22461A>T	XP_006715473.1:p.Thr7487=
XM_006715411.1:c.22410A>T	XP_006715474.1:p.Thr7470=
XM_006715412.1:c.22446A>T	XP_006715475.1:p.Thr7482=
XM_006715413.1:c.22461A>T	XP_006715476.1:p.Thr7487=
XM_006715414.1:c.22389A>T	XP_006715477.1:p.Thr7463=
XM_006715415.1:c.22461A>T	XP_006715478.1:p.Thr7487=
XM_006715416.1:c.22446A>T	XP_006715479.1:p.Thr7482=
XM_006715417.1:c.22320A>T	XP_006715480.1:p.Thr7440=
XM_006715420.1:c.22308A>T	XP_006715483.1:p.Thr7436=
XM_006715421.1:c.22305A>T	XP_006715484.1:p.Thr7435=
XM_006715422.1:c.22302A>T	XP_006715485.1:p.Thr7434=
XM_006715423.1:c.22461A>T	XP_006715486.1:p.Thr7487=
XM_006715424.1:c.22461A>T	XP_006715487.1:p.Thr7487=
XM_006715425.1:c.22461A>T	XP_006715488.1:p.Thr7487=
XM_011535641.1:c.22458A>T	XP_011533943.1:p.Thr7486=
XM_011535642.1:c.22446A>T	XP_011533944.1:p.Thr7482=
XM_011535643.1:c.22296A>T	XP_011533945.1:p.Thr7432=
XM_011535644.1:c.20736A>T	XP_011533946.1:p.Thr6912=
XM_011535645.1:c.20229A>T	XP_011533947.1:p.Thr6743=
XM_011535647.1:c.15696A>T	XP_011533949.1:p.Thr5232=
XM_006715408.2:c.22449A>T	XP_006715471.1:p.Thr7483=
XM_006715410.2:c.22461A>T	XP_006715473.1:p.Thr7487=
XM_006715412.2:c.22446A>T	XP_006715475.1:p.Thr7482=
XM_006715413.2:c.22461A>T	XP_006715476.1:p.Thr7487=
XM_006715415.2:c.22461A>T	XP_006715478.1:p.Thr7487=
XM_006715416.2:c.22446A>T	XP_006715479.1:p.Thr7482=
XM_006715417.2:c.22320A>T	XP_006715480.1:p.Thr7440=
XM_006715420.2:c.22308A>T	XP_006715483.1:p.Thr7436=
XM_006715421.2:c.22305A>T	XP_006715484.1:p.Thr7435=
XM_006715423.2:c.22461A>T	XP_006715486.1:p.Thr7487=
XM_006715424.2:c.22461A>T	XP_006715487.1:p.Thr7487=
XM_006715425.2:c.22461A>T	XP_006715488.1:p.Thr7487=
XM_011535641.2:c.22458A>T	XP_011533943.1:p.Thr7486=
XM_011535642.2:c.22446A>T	XP_011533944.1:p.Thr7482=
XM_011535645.2:c.20229A>T	XP_011533947.1:p.Thr6743=
XM_017010608.1:c.22461A>T	XP_016866097.1:p.Thr7487=
XM_017010609.1:c.22461A>T	XP_016866098.1:p.Thr7487=
XM_017010610.1:c.22440A>T	XP_016866099.1:p.Thr7480=
XM_017010611.2:c.22434A>T	XP_016866100.1:p.Thr7478=
XM_017010612.1:c.22383A>T	XP_016866101.1:p.Thr7461=
XM_017010613.1:c.22458A>T	XP_016866102.1:p.Thr7486=
XM_017010614.1:c.22305A>T	XP_016866103.1:p.Thr7435=
XM_017010615.1:c.22305A>T	XP_016866104.1:p.Thr7435=
XM_017010616.1:c.22461A>T	XP_016866105.1:p.Thr7487=
XM_017010617.1:c.22458A>T	XP_016866106.1:p.Thr7486=
XM_017010618.1:c.22446A>T	XP_016866107.1:p.Thr7482=
XM_017010619.1:c.20736A>T	XP_016866108.1:p.Thr6912=
NM_182961.4:c.22425A>T MANE Select	NP_892006.3:p.Thr7475=
NM_033071.5:c.22212A>T	NP_149062.2:p.Thr7404=