Canonical Allele Identifier: CA1673206260

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140027C= , CM000668.2:g.152140027C=	GRCh38
NC_000006.11:g.152461162C= , CM000668.1:g.152461162C=	GRCh37
NC_000006.10:g.152502855C=	NCBI36
NG_012855.1:g.502373G=
NG_012855.2:g.502373G=

Transcript Alleles

HGVS	Amino-acid Change
NM_182961.4:c.25381G= MANE Select	NP_892006.3:p.Glu8461=
ENST00000367255.10:c.25381G= MANE Select	ENSP00000356224.5:p.Glu8461=
NM_001347702.2:c.1915G= MANE Plus Clinical	NP_001334631.1:p.Glu639=
ENST00000354674.5:c.1915G= MANE Plus Clinical	ENSP00000346701.4:p.Glu639=
NM_001347701.1:c.1987G=	NP_001334630.1:p.Glu663=
NM_001347701.2:c.1987G=	NP_001334630.1:p.Glu663=
NM_001347702.1:c.1915G=	NP_001334631.1:p.Glu639=
NM_033071.3:c.25237G=	NP_149062.1:p.Glu8413=
NM_033071.5:c.25237G=	NP_149062.2:p.Glu8413=
NM_182961.3:c.25381G=	NP_892006.3:p.Glu8461=
ENST00000341594.9:c.24166G=	ENSP00000341887.6:p.Glu8056=
ENST00000347037.9:n.2129G=
ENST00000354674.4:c.1915G=	ENSP00000346701.4:p.Glu639=
ENST00000367251.7:c.4216G=	ENSP00000356220.3:p.Glu1406=
ENST00000367255.9:c.25381G=	ENSP00000356224.5:p.Glu8461=
ENST00000367256.9:n.9073G=
ENST00000367257.8:c.3319G=	ENSP00000356226.4:p.Glu1107=
ENST00000409694.6:n.8965G=
ENST00000423061.5:c.25237G=	ENSP00000396024.1:p.Glu8413=
ENST00000423061.6:c.25237G=	ENSP00000396024.1:p.Glu8413=
ENST00000460912.6:n.1995G=
ENST00000478916.5:n.4403G=
ENST00000536990.5:n.2218G=
ENST00000539504.5:c.1846G=	ENSP00000441052.1:p.Glu616=
ENST00000672154.1:c.783G=
ENST00000672169.1:c.1116G=
ENST00000673173.1:c.1025G=
ENST00000673451.1:c.1153G=	ENSP00000500189.1:p.Glu385=
XM_006715407.1:c.25486G=	XP_006715470.1:p.Glu8496=
XM_006715408.1:c.25474G=	XP_006715471.1:p.Glu8492=
XM_006715408.2:c.25474G=	XP_006715471.1:p.Glu8492=
XM_006715409.1:c.25465G=	XP_006715472.1:p.Glu8489=
XM_006715410.1:c.25486G=	XP_006715473.1:p.Glu8496=
XM_006715410.2:c.25486G=	XP_006715473.1:p.Glu8496=
XM_006715411.1:c.25435G=	XP_006715474.1:p.Glu8479=
XM_006715412.1:c.25471G=	XP_006715475.1:p.Glu8491=
XM_006715412.2:c.25471G=	XP_006715475.1:p.Glu8491=
XM_006715413.1:c.25417G=	XP_006715476.1:p.Glu8473=
XM_006715413.2:c.25417G=	XP_006715476.1:p.Glu8473=
XM_006715414.1:c.25414G=	XP_006715477.1:p.Glu8472=
XM_006715415.1:c.25417G=	XP_006715478.1:p.Glu8473=
XM_006715415.2:c.25417G=	XP_006715478.1:p.Glu8473=
XM_006715416.1:c.25402G=	XP_006715479.1:p.Glu8468=
XM_006715416.2:c.25402G=	XP_006715479.1:p.Glu8468=
XM_006715417.1:c.25345G=	XP_006715480.1:p.Glu8449=
XM_006715417.2:c.25345G=	XP_006715480.1:p.Glu8449=
XM_006715420.1:c.25333G=	XP_006715483.1:p.Glu8445=
XM_006715420.2:c.25333G=	XP_006715483.1:p.Glu8445=
XM_006715421.1:c.25330G=	XP_006715484.1:p.Glu8444=
XM_006715421.2:c.25330G=	XP_006715484.1:p.Glu8444=
XM_006715422.1:c.25327G=	XP_006715485.1:p.Glu8443=
XM_006715423.1:c.25486G=	XP_006715486.1:p.Glu8496=
XM_006715423.2:c.25486G=	XP_006715486.1:p.Glu8496=
XM_006715424.1:c.25486G=	XP_006715487.1:p.Glu8496=
XM_006715424.2:c.25486G=	XP_006715487.1:p.Glu8496=
XM_006715425.1:c.25417G=	XP_006715488.1:p.Glu8473=
XM_006715425.2:c.25417G=	XP_006715488.1:p.Glu8473=
XM_011535641.1:c.25483G=	XP_011533943.1:p.Glu8495=
XM_011535641.2:c.25483G=	XP_011533943.1:p.Glu8495=
XM_011535642.1:c.25471G=	XP_011533944.1:p.Glu8491=
XM_011535642.2:c.25471G=	XP_011533944.1:p.Glu8491=
XM_011535643.1:c.25321G=	XP_011533945.1:p.Glu8441=
XM_011535644.1:c.23761G=	XP_011533946.1:p.Glu7921=
XM_011535645.1:c.23254G=	XP_011533947.1:p.Glu7752=
XM_011535645.2:c.23254G=	XP_011533947.1:p.Glu7752=
XM_011535647.1:c.18721G=	XP_011533949.1:p.Glu6241=
XM_017010608.1:c.25486G=	XP_016866097.1:p.Glu8496=
XM_017010609.1:c.25486G=	XP_016866098.1:p.Glu8496=
XM_017010610.1:c.25465G=	XP_016866099.1:p.Glu8489=
XM_017010611.2:c.25459G=	XP_016866100.1:p.Glu8487=
XM_017010612.1:c.25408G=	XP_016866101.1:p.Glu8470=
XM_017010613.1:c.25414G=	XP_016866102.1:p.Glu8472=
XM_017010614.1:c.25330G=	XP_016866103.1:p.Glu8444=
XM_017010615.1:c.25261G=	XP_016866104.1:p.Glu8421=
XM_017010616.1:c.25417G=	XP_016866105.1:p.Glu8473=
XM_017010617.1:c.25414G=	XP_016866106.1:p.Glu8472=
XM_017010618.1:c.25402G=	XP_016866107.1:p.Glu8468=
XM_017010619.1:c.23761G=	XP_016866108.1:p.Glu7921=