Canonical Allele Identifier: CA1673206282

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140038C= , CM000668.2:g.152140038C=	GRCh38
NC_000006.11:g.152461173C= , CM000668.1:g.152461173C=	GRCh37
NC_000006.10:g.152502866C=	NCBI36
NG_012855.1:g.502362G=
NG_012855.2:g.502362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1904G= MANE Plus Clinical	ENSP00000346701.4:p.Gly635=
ENST00000367255.10:c.25370G= MANE Select	ENSP00000356224.5:p.Gly8457=
ENST00000423061.6:c.25226G=	ENSP00000396024.1:p.Gly8409=
ENST00000672154.1:c.772G=
ENST00000672169.1:c.1105G=
ENST00000673173.1:c.1014G=
ENST00000673451.1:c.1142G=	ENSP00000500189.1:p.Gly381=
ENST00000341594.9:c.24155G=	ENSP00000341887.6:p.Gly8052=
ENST00000347037.9:n.2118G=
ENST00000354674.4:c.1904G=	ENSP00000346701.4:p.Gly635=
ENST00000367251.7:c.4205G=	ENSP00000356220.3:p.Gly1402=
ENST00000367255.9:c.25370G=	ENSP00000356224.5:p.Gly8457=
ENST00000367256.9:n.9062G=
ENST00000367257.8:c.3308G=	ENSP00000356226.4:p.Gly1103=
ENST00000409694.6:n.8954G=
ENST00000423061.5:c.25226G=	ENSP00000396024.1:p.Gly8409=
ENST00000460912.6:n.1984G=
ENST00000478916.5:n.4392G=
ENST00000536990.5:n.2207G=
ENST00000539504.5:c.1835G=	ENSP00000441052.1:p.Gly612=
NM_033071.3:c.25226G=	NP_149062.1:p.Gly8409=
NM_182961.3:c.25370G=	NP_892006.3:p.Gly8457=
XM_006715407.1:c.25475G=	XP_006715470.1:p.Gly8492=
XM_006715408.1:c.25463G=	XP_006715471.1:p.Gly8488=
XM_006715409.1:c.25454G=	XP_006715472.1:p.Gly8485=
XM_006715410.1:c.25475G=	XP_006715473.1:p.Gly8492=
XM_006715411.1:c.25424G=	XP_006715474.1:p.Gly8475=
XM_006715412.1:c.25460G=	XP_006715475.1:p.Gly8487=
XM_006715413.1:c.25406G=	XP_006715476.1:p.Gly8469=
XM_006715414.1:c.25403G=	XP_006715477.1:p.Gly8468=
XM_006715415.1:c.25406G=	XP_006715478.1:p.Gly8469=
XM_006715416.1:c.25391G=	XP_006715479.1:p.Gly8464=
XM_006715417.1:c.25334G=	XP_006715480.1:p.Gly8445=
XM_006715420.1:c.25322G=	XP_006715483.1:p.Gly8441=
XM_006715421.1:c.25319G=	XP_006715484.1:p.Gly8440=
XM_006715422.1:c.25316G=	XP_006715485.1:p.Gly8439=
XM_006715423.1:c.25475G=	XP_006715486.1:p.Gly8492=
XM_006715424.1:c.25475G=	XP_006715487.1:p.Gly8492=
XM_006715425.1:c.25406G=	XP_006715488.1:p.Gly8469=
XM_011535641.1:c.25472G=	XP_011533943.1:p.Gly8491=
XM_011535642.1:c.25460G=	XP_011533944.1:p.Gly8487=
XM_011535643.1:c.25310G=	XP_011533945.1:p.Gly8437=
XM_011535644.1:c.23750G=	XP_011533946.1:p.Gly7917=
XM_011535645.1:c.23243G=	XP_011533947.1:p.Gly7748=
XM_011535647.1:c.18710G=	XP_011533949.1:p.Gly6237=
NM_001347701.1:c.1976G=	NP_001334630.1:p.Gly659=
NM_001347702.1:c.1904G=	NP_001334631.1:p.Gly635=
XM_006715408.2:c.25463G=	XP_006715471.1:p.Gly8488=
XM_006715410.2:c.25475G=	XP_006715473.1:p.Gly8492=
XM_006715412.2:c.25460G=	XP_006715475.1:p.Gly8487=
XM_006715413.2:c.25406G=	XP_006715476.1:p.Gly8469=
XM_006715415.2:c.25406G=	XP_006715478.1:p.Gly8469=
XM_006715416.2:c.25391G=	XP_006715479.1:p.Gly8464=
XM_006715417.2:c.25334G=	XP_006715480.1:p.Gly8445=
XM_006715420.2:c.25322G=	XP_006715483.1:p.Gly8441=
XM_006715421.2:c.25319G=	XP_006715484.1:p.Gly8440=
XM_006715423.2:c.25475G=	XP_006715486.1:p.Gly8492=
XM_006715424.2:c.25475G=	XP_006715487.1:p.Gly8492=
XM_006715425.2:c.25406G=	XP_006715488.1:p.Gly8469=
XM_011535641.2:c.25472G=	XP_011533943.1:p.Gly8491=
XM_011535642.2:c.25460G=	XP_011533944.1:p.Gly8487=
XM_011535645.2:c.23243G=	XP_011533947.1:p.Gly7748=
XM_017010608.1:c.25475G=	XP_016866097.1:p.Gly8492=
XM_017010609.1:c.25475G=	XP_016866098.1:p.Gly8492=
XM_017010610.1:c.25454G=	XP_016866099.1:p.Gly8485=
XM_017010611.2:c.25448G=	XP_016866100.1:p.Gly8483=
XM_017010612.1:c.25397G=	XP_016866101.1:p.Gly8466=
XM_017010613.1:c.25403G=	XP_016866102.1:p.Gly8468=
XM_017010614.1:c.25319G=	XP_016866103.1:p.Gly8440=
XM_017010615.1:c.25250G=	XP_016866104.1:p.Gly8417=
XM_017010616.1:c.25406G=	XP_016866105.1:p.Gly8469=
XM_017010617.1:c.25403G=	XP_016866106.1:p.Gly8468=
XM_017010618.1:c.25391G=	XP_016866107.1:p.Gly8464=
XM_017010619.1:c.23750G=	XP_016866108.1:p.Gly7917=
NM_182961.4:c.25370G= MANE Select	NP_892006.3:p.Gly8457=
NM_001347701.2:c.1976G=	NP_001334630.1:p.Gly659=
NM_001347702.2:c.1904G= MANE Plus Clinical	NP_001334631.1:p.Gly635=
NM_033071.5:c.25226G=	NP_149062.2:p.Gly8409=