Canonical Allele Identifier: CA452969945

Gene: SYNE1

Linked Data

• dbSNP Id: rs1442695481
• gnomAD v4: 6-152140106-C-T
• MyVariant Identifiers: chr6:g.152461241C>T (hg19) ; chr6:g.152140106C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140106C>T , CM000668.2:g.152140106C>T	GRCh38
NC_000006.11:g.152461241C>T , CM000668.1:g.152461241C>T	GRCh37
NC_000006.10:g.152502934C>T	NCBI36
NG_012855.1:g.502294G>A
NG_012855.2:g.502294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1836G>A MANE Plus Clinical	ENSP00000346701.4:p.Arg612=
ENST00000367255.10:c.25302G>A MANE Select	ENSP00000356224.5:p.Arg8434=
ENST00000423061.6:c.25158G>A	ENSP00000396024.1:p.Arg8386=
ENST00000672154.1:c.704G>A
ENST00000672169.1:c.1037G>A
ENST00000673173.1:c.946G>A
ENST00000673451.1:c.1074G>A	ENSP00000500189.1:p.Arg358=
ENST00000341594.9:c.24087G>A	ENSP00000341887.6:p.Arg8029=
ENST00000347037.9:n.2050G>A
ENST00000354674.4:c.1836G>A	ENSP00000346701.4:p.Arg612=
ENST00000367251.7:c.4137G>A	ENSP00000356220.3:p.Arg1379=
ENST00000367255.9:c.25302G>A	ENSP00000356224.5:p.Arg8434=
ENST00000367256.9:n.8994G>A
ENST00000367257.8:c.3240G>A	ENSP00000356226.4:p.Arg1080=
ENST00000409694.6:n.8886G>A
ENST00000423061.5:c.25158G>A	ENSP00000396024.1:p.Arg8386=
ENST00000460912.6:n.1916G>A
ENST00000478916.5:n.4324G>A
ENST00000536990.5:n.2139G>A
ENST00000539504.5:c.1767G>A	ENSP00000441052.1:p.Arg589=
NM_033071.3:c.25158G>A	NP_149062.1:p.Arg8386=
NM_182961.3:c.25302G>A	NP_892006.3:p.Arg8434=
XM_006715407.1:c.25407G>A	XP_006715470.1:p.Arg8469=
XM_006715408.1:c.25395G>A	XP_006715471.1:p.Arg8465=
XM_006715409.1:c.25386G>A	XP_006715472.1:p.Arg8462=
XM_006715410.1:c.25407G>A	XP_006715473.1:p.Arg8469=
XM_006715411.1:c.25356G>A	XP_006715474.1:p.Arg8452=
XM_006715412.1:c.25392G>A	XP_006715475.1:p.Arg8464=
XM_006715413.1:c.25338G>A	XP_006715476.1:p.Arg8446=
XM_006715414.1:c.25335G>A	XP_006715477.1:p.Arg8445=
XM_006715415.1:c.25338G>A	XP_006715478.1:p.Arg8446=
XM_006715416.1:c.25323G>A	XP_006715479.1:p.Arg8441=
XM_006715417.1:c.25266G>A	XP_006715480.1:p.Arg8422=
XM_006715420.1:c.25254G>A	XP_006715483.1:p.Arg8418=
XM_006715421.1:c.25251G>A	XP_006715484.1:p.Arg8417=
XM_006715422.1:c.25248G>A	XP_006715485.1:p.Arg8416=
XM_006715423.1:c.25407G>A	XP_006715486.1:p.Arg8469=
XM_006715424.1:c.25407G>A	XP_006715487.1:p.Arg8469=
XM_006715425.1:c.25338G>A	XP_006715488.1:p.Arg8446=
XM_011535641.1:c.25404G>A	XP_011533943.1:p.Arg8468=
XM_011535642.1:c.25392G>A	XP_011533944.1:p.Arg8464=
XM_011535643.1:c.25242G>A	XP_011533945.1:p.Arg8414=
XM_011535644.1:c.23682G>A	XP_011533946.1:p.Arg7894=
XM_011535645.1:c.23175G>A	XP_011533947.1:p.Arg7725=
XM_011535647.1:c.18642G>A	XP_011533949.1:p.Arg6214=
NM_001347701.1:c.1908G>A	NP_001334630.1:p.Arg636=
NM_001347702.1:c.1836G>A	NP_001334631.1:p.Arg612=
XM_006715408.2:c.25395G>A	XP_006715471.1:p.Arg8465=
XM_006715410.2:c.25407G>A	XP_006715473.1:p.Arg8469=
XM_006715412.2:c.25392G>A	XP_006715475.1:p.Arg8464=
XM_006715413.2:c.25338G>A	XP_006715476.1:p.Arg8446=
XM_006715415.2:c.25338G>A	XP_006715478.1:p.Arg8446=
XM_006715416.2:c.25323G>A	XP_006715479.1:p.Arg8441=
XM_006715417.2:c.25266G>A	XP_006715480.1:p.Arg8422=
XM_006715420.2:c.25254G>A	XP_006715483.1:p.Arg8418=
XM_006715421.2:c.25251G>A	XP_006715484.1:p.Arg8417=
XM_006715423.2:c.25407G>A	XP_006715486.1:p.Arg8469=
XM_006715424.2:c.25407G>A	XP_006715487.1:p.Arg8469=
XM_006715425.2:c.25338G>A	XP_006715488.1:p.Arg8446=
XM_011535641.2:c.25404G>A	XP_011533943.1:p.Arg8468=
XM_011535642.2:c.25392G>A	XP_011533944.1:p.Arg8464=
XM_011535645.2:c.23175G>A	XP_011533947.1:p.Arg7725=
XM_017010608.1:c.25407G>A	XP_016866097.1:p.Arg8469=
XM_017010609.1:c.25407G>A	XP_016866098.1:p.Arg8469=
XM_017010610.1:c.25386G>A	XP_016866099.1:p.Arg8462=
XM_017010611.2:c.25380G>A	XP_016866100.1:p.Arg8460=
XM_017010612.1:c.25329G>A	XP_016866101.1:p.Arg8443=
XM_017010613.1:c.25335G>A	XP_016866102.1:p.Arg8445=
XM_017010614.1:c.25251G>A	XP_016866103.1:p.Arg8417=
XM_017010615.1:c.25182G>A	XP_016866104.1:p.Arg8394=
XM_017010616.1:c.25338G>A	XP_016866105.1:p.Arg8446=
XM_017010617.1:c.25335G>A	XP_016866106.1:p.Arg8445=
XM_017010618.1:c.25323G>A	XP_016866107.1:p.Arg8441=
XM_017010619.1:c.23682G>A	XP_016866108.1:p.Arg7894=
NM_182961.4:c.25302G>A MANE Select	NP_892006.3:p.Arg8434=
NM_001347701.2:c.1908G>A	NP_001334630.1:p.Arg636=
NM_001347702.2:c.1836G>A MANE Plus Clinical	NP_001334631.1:p.Arg612=
NM_033071.5:c.25158G>A	NP_149062.2:p.Arg8386=