Canonical Allele Identifier: CA1673241121

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213698C= , CM000668.2:g.152213698C=	GRCh38
NC_000006.11:g.152534833C= , CM000668.1:g.152534833C=	GRCh37
NC_000006.10:g.152576526C=	NCBI36
NG_012855.1:g.428702G=
NG_012855.2:g.428702G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22408G= MANE Select	ENSP00000356224.5:p.Glu7470=
ENST00000423061.6:c.22195G=	ENSP00000396024.1:p.Glu7399=
ENST00000341594.9:c.21193G=	ENSP00000341887.6:p.Glu7065=
ENST00000367251.7:c.1174G=	ENSP00000356220.3:p.Glu392=
ENST00000367255.9:c.22408G=	ENSP00000356224.5:p.Glu7470=
ENST00000367256.9:n.6100G=
ENST00000367257.8:c.346G=	ENSP00000356226.4:p.Glu116=
ENST00000409694.6:n.5992G=
ENST00000423061.5:c.22195G=	ENSP00000396024.1:p.Glu7399=
NM_033071.3:c.22195G=	NP_149062.1:p.Glu7399=
NM_182961.3:c.22408G=	NP_892006.3:p.Glu7470=
XM_006715407.1:c.22444G=	XP_006715470.1:p.Glu7482=
XM_006715408.1:c.22432G=	XP_006715471.1:p.Glu7478=
XM_006715409.1:c.22423G=	XP_006715472.1:p.Glu7475=
XM_006715410.1:c.22444G=	XP_006715473.1:p.Glu7482=
XM_006715411.1:c.22393G=	XP_006715474.1:p.Glu7465=
XM_006715412.1:c.22429G=	XP_006715475.1:p.Glu7477=
XM_006715413.1:c.22444G=	XP_006715476.1:p.Glu7482=
XM_006715414.1:c.22372G=	XP_006715477.1:p.Glu7458=
XM_006715415.1:c.22444G=	XP_006715478.1:p.Glu7482=
XM_006715416.1:c.22429G=	XP_006715479.1:p.Glu7477=
XM_006715417.1:c.22303G=	XP_006715480.1:p.Glu7435=
XM_006715420.1:c.22291G=	XP_006715483.1:p.Glu7431=
XM_006715421.1:c.22288G=	XP_006715484.1:p.Glu7430=
XM_006715422.1:c.22285G=	XP_006715485.1:p.Glu7429=
XM_006715423.1:c.22444G=	XP_006715486.1:p.Glu7482=
XM_006715424.1:c.22444G=	XP_006715487.1:p.Glu7482=
XM_006715425.1:c.22444G=	XP_006715488.1:p.Glu7482=
XM_011535641.1:c.22441G=	XP_011533943.1:p.Glu7481=
XM_011535642.1:c.22429G=	XP_011533944.1:p.Glu7477=
XM_011535643.1:c.22279G=	XP_011533945.1:p.Glu7427=
XM_011535644.1:c.20719G=	XP_011533946.1:p.Glu6907=
XM_011535645.1:c.20212G=	XP_011533947.1:p.Glu6738=
XM_011535647.1:c.15679G=	XP_011533949.1:p.Glu5227=
XM_006715408.2:c.22432G=	XP_006715471.1:p.Glu7478=
XM_006715410.2:c.22444G=	XP_006715473.1:p.Glu7482=
XM_006715412.2:c.22429G=	XP_006715475.1:p.Glu7477=
XM_006715413.2:c.22444G=	XP_006715476.1:p.Glu7482=
XM_006715415.2:c.22444G=	XP_006715478.1:p.Glu7482=
XM_006715416.2:c.22429G=	XP_006715479.1:p.Glu7477=
XM_006715417.2:c.22303G=	XP_006715480.1:p.Glu7435=
XM_006715420.2:c.22291G=	XP_006715483.1:p.Glu7431=
XM_006715421.2:c.22288G=	XP_006715484.1:p.Glu7430=
XM_006715423.2:c.22444G=	XP_006715486.1:p.Glu7482=
XM_006715424.2:c.22444G=	XP_006715487.1:p.Glu7482=
XM_006715425.2:c.22444G=	XP_006715488.1:p.Glu7482=
XM_011535641.2:c.22441G=	XP_011533943.1:p.Glu7481=
XM_011535642.2:c.22429G=	XP_011533944.1:p.Glu7477=
XM_011535645.2:c.20212G=	XP_011533947.1:p.Glu6738=
XM_017010608.1:c.22444G=	XP_016866097.1:p.Glu7482=
XM_017010609.1:c.22444G=	XP_016866098.1:p.Glu7482=
XM_017010610.1:c.22423G=	XP_016866099.1:p.Glu7475=
XM_017010611.2:c.22417G=	XP_016866100.1:p.Glu7473=
XM_017010612.1:c.22366G=	XP_016866101.1:p.Glu7456=
XM_017010613.1:c.22441G=	XP_016866102.1:p.Glu7481=
XM_017010614.1:c.22288G=	XP_016866103.1:p.Glu7430=
XM_017010615.1:c.22288G=	XP_016866104.1:p.Glu7430=
XM_017010616.1:c.22444G=	XP_016866105.1:p.Glu7482=
XM_017010617.1:c.22441G=	XP_016866106.1:p.Glu7481=
XM_017010618.1:c.22429G=	XP_016866107.1:p.Glu7477=
XM_017010619.1:c.20719G=	XP_016866108.1:p.Glu6907=
NM_182961.4:c.22408G= MANE Select	NP_892006.3:p.Glu7470=
NM_033071.5:c.22195G=	NP_149062.2:p.Glu7399=