Canonical Allele Identifier: CA366099520

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534869G>T (hg19) ; chr6:g.152213734G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213734G>T , CM000668.2:g.152213734G>T	GRCh38
NC_000006.11:g.152534869G>T , CM000668.1:g.152534869G>T	GRCh37
NC_000006.10:g.152576562G>T	NCBI36
NG_012855.1:g.428666C>A
NG_012855.2:g.428666C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22372C>A MANE Select	ENSP00000356224.5:p.His7458Asn
ENST00000423061.6:c.22159C>A	ENSP00000396024.1:p.His7387Asn
ENST00000341594.9:c.21157C>A	ENSP00000341887.6:p.His7053Asn
ENST00000367251.7:c.1138C>A	ENSP00000356220.3:p.His380Asn
ENST00000367255.9:c.22372C>A	ENSP00000356224.5:p.His7458Asn
ENST00000367256.9:n.6064C>A
ENST00000367257.8:c.310C>A	ENSP00000356226.4:p.His104Asn
ENST00000409694.6:n.5956C>A
ENST00000423061.5:c.22159C>A	ENSP00000396024.1:p.His7387Asn
NM_033071.3:c.22159C>A	NP_149062.1:p.His7387Asn
NM_182961.3:c.22372C>A	NP_892006.3:p.His7458Asn
XM_006715407.1:c.22408C>A	XP_006715470.1:p.His7470Asn
XM_006715408.1:c.22396C>A	XP_006715471.1:p.His7466Asn
XM_006715409.1:c.22387C>A	XP_006715472.1:p.His7463Asn
XM_006715410.1:c.22408C>A	XP_006715473.1:p.His7470Asn
XM_006715411.1:c.22357C>A	XP_006715474.1:p.His7453Asn
XM_006715412.1:c.22393C>A	XP_006715475.1:p.His7465Asn
XM_006715413.1:c.22408C>A	XP_006715476.1:p.His7470Asn
XM_006715414.1:c.22336C>A	XP_006715477.1:p.His7446Asn
XM_006715415.1:c.22408C>A	XP_006715478.1:p.His7470Asn
XM_006715416.1:c.22393C>A	XP_006715479.1:p.His7465Asn
XM_006715417.1:c.22267C>A	XP_006715480.1:p.His7423Asn
XM_006715420.1:c.22255C>A	XP_006715483.1:p.His7419Asn
XM_006715421.1:c.22252C>A	XP_006715484.1:p.His7418Asn
XM_006715422.1:c.22249C>A	XP_006715485.1:p.His7417Asn
XM_006715423.1:c.22408C>A	XP_006715486.1:p.His7470Asn
XM_006715424.1:c.22408C>A	XP_006715487.1:p.His7470Asn
XM_006715425.1:c.22408C>A	XP_006715488.1:p.His7470Asn
XM_011535641.1:c.22405C>A	XP_011533943.1:p.His7469Asn
XM_011535642.1:c.22393C>A	XP_011533944.1:p.His7465Asn
XM_011535643.1:c.22243C>A	XP_011533945.1:p.His7415Asn
XM_011535644.1:c.20683C>A	XP_011533946.1:p.His6895Asn
XM_011535645.1:c.20176C>A	XP_011533947.1:p.His6726Asn
XM_011535647.1:c.15643C>A	XP_011533949.1:p.His5215Asn
XM_006715408.2:c.22396C>A	XP_006715471.1:p.His7466Asn
XM_006715410.2:c.22408C>A	XP_006715473.1:p.His7470Asn
XM_006715412.2:c.22393C>A	XP_006715475.1:p.His7465Asn
XM_006715413.2:c.22408C>A	XP_006715476.1:p.His7470Asn
XM_006715415.2:c.22408C>A	XP_006715478.1:p.His7470Asn
XM_006715416.2:c.22393C>A	XP_006715479.1:p.His7465Asn
XM_006715417.2:c.22267C>A	XP_006715480.1:p.His7423Asn
XM_006715420.2:c.22255C>A	XP_006715483.1:p.His7419Asn
XM_006715421.2:c.22252C>A	XP_006715484.1:p.His7418Asn
XM_006715423.2:c.22408C>A	XP_006715486.1:p.His7470Asn
XM_006715424.2:c.22408C>A	XP_006715487.1:p.His7470Asn
XM_006715425.2:c.22408C>A	XP_006715488.1:p.His7470Asn
XM_011535641.2:c.22405C>A	XP_011533943.1:p.His7469Asn
XM_011535642.2:c.22393C>A	XP_011533944.1:p.His7465Asn
XM_011535645.2:c.20176C>A	XP_011533947.1:p.His6726Asn
XM_017010608.1:c.22408C>A	XP_016866097.1:p.His7470Asn
XM_017010609.1:c.22408C>A	XP_016866098.1:p.His7470Asn
XM_017010610.1:c.22387C>A	XP_016866099.1:p.His7463Asn
XM_017010611.2:c.22381C>A	XP_016866100.1:p.His7461Asn
XM_017010612.1:c.22330C>A	XP_016866101.1:p.His7444Asn
XM_017010613.1:c.22405C>A	XP_016866102.1:p.His7469Asn
XM_017010614.1:c.22252C>A	XP_016866103.1:p.His7418Asn
XM_017010615.1:c.22252C>A	XP_016866104.1:p.His7418Asn
XM_017010616.1:c.22408C>A	XP_016866105.1:p.His7470Asn
XM_017010617.1:c.22405C>A	XP_016866106.1:p.His7469Asn
XM_017010618.1:c.22393C>A	XP_016866107.1:p.His7465Asn
XM_017010619.1:c.20683C>A	XP_016866108.1:p.His6895Asn
NM_182961.4:c.22372C>A MANE Select	NP_892006.3:p.His7458Asn
NM_033071.5:c.22159C>A	NP_149062.2:p.His7387Asn