Canonical Allele Identifier: CA452747213

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152464781G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152143646G>A , CM000668.2:g.152143646G>A	GRCh38
NC_000006.11:g.152464781G>A , CM000668.1:g.152464781G>A	GRCh37
NC_000006.10:g.152506474G>A	NCBI36
NG_012855.1:g.498754C>T
NG_012855.2:g.498754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1630C>T MANE Plus Clinical	ENSP00000346701.4:p.Leu544=
ENST00000367255.10:c.25096C>T MANE Select	ENSP00000356224.5:p.Leu8366=
ENST00000423061.6:c.24952C>T	ENSP00000396024.1:p.Leu8318=
ENST00000672154.1:c.498C>T
ENST00000672169.1:c.831C>T
ENST00000673173.1:c.891-3485C>T
ENST00000673451.1:c.868C>T	ENSP00000500189.1:p.Leu290=
ENST00000341594.9:c.23881C>T	ENSP00000341887.6:p.Leu7961=
ENST00000347037.9:n.1844C>T
ENST00000354674.4:c.1630C>T	ENSP00000346701.4:p.Leu544=
ENST00000367251.7:c.3931C>T	ENSP00000356220.3:p.Leu1311=
ENST00000367255.9:c.25096C>T	ENSP00000356224.5:p.Leu8366=
ENST00000367256.9:n.8788C>T
ENST00000367257.8:c.3034C>T	ENSP00000356226.4:p.Leu1012=
ENST00000409694.6:n.8680C>T
ENST00000423061.5:c.24952C>T	ENSP00000396024.1:p.Leu8318=
ENST00000460912.6:n.1710C>T
ENST00000478916.5:n.4118C>T
ENST00000536990.5:n.1933C>T
ENST00000539504.5:c.1561C>T	ENSP00000441052.1:p.Leu521=
NM_033071.3:c.24952C>T	NP_149062.1:p.Leu8318=
NM_182961.3:c.25096C>T	NP_892006.3:p.Leu8366=
XM_006715407.1:c.25201C>T	XP_006715470.1:p.Leu8401=
XM_006715408.1:c.25189C>T	XP_006715471.1:p.Leu8397=
XM_006715409.1:c.25180C>T	XP_006715472.1:p.Leu8394=
XM_006715410.1:c.25201C>T	XP_006715473.1:p.Leu8401=
XM_006715411.1:c.25150C>T	XP_006715474.1:p.Leu8384=
XM_006715412.1:c.25186C>T	XP_006715475.1:p.Leu8396=
XM_006715413.1:c.25132C>T	XP_006715476.1:p.Leu8378=
XM_006715414.1:c.25129C>T	XP_006715477.1:p.Leu8377=
XM_006715415.1:c.25132C>T	XP_006715478.1:p.Leu8378=
XM_006715416.1:c.25117C>T	XP_006715479.1:p.Leu8373=
XM_006715417.1:c.25060C>T	XP_006715480.1:p.Leu8354=
XM_006715420.1:c.25048C>T	XP_006715483.1:p.Leu8350=
XM_006715421.1:c.25045C>T	XP_006715484.1:p.Leu8349=
XM_006715422.1:c.25042C>T	XP_006715485.1:p.Leu8348=
XM_006715423.1:c.25201C>T	XP_006715486.1:p.Leu8401=
XM_006715424.1:c.25201C>T	XP_006715487.1:p.Leu8401=
XM_006715425.1:c.25132C>T	XP_006715488.1:p.Leu8378=
XM_011535641.1:c.25198C>T	XP_011533943.1:p.Leu8400=
XM_011535642.1:c.25186C>T	XP_011533944.1:p.Leu8396=
XM_011535643.1:c.25036C>T	XP_011533945.1:p.Leu8346=
XM_011535644.1:c.23476C>T	XP_011533946.1:p.Leu7826=
XM_011535645.1:c.22969C>T	XP_011533947.1:p.Leu7657=
XM_011535647.1:c.18436C>T	XP_011533949.1:p.Leu6146=
NM_001347701.1:c.1702C>T	NP_001334630.1:p.Leu568=
NM_001347702.1:c.1630C>T	NP_001334631.1:p.Leu544=
XM_006715408.2:c.25189C>T	XP_006715471.1:p.Leu8397=
XM_006715410.2:c.25201C>T	XP_006715473.1:p.Leu8401=
XM_006715412.2:c.25186C>T	XP_006715475.1:p.Leu8396=
XM_006715413.2:c.25132C>T	XP_006715476.1:p.Leu8378=
XM_006715415.2:c.25132C>T	XP_006715478.1:p.Leu8378=
XM_006715416.2:c.25117C>T	XP_006715479.1:p.Leu8373=
XM_006715417.2:c.25060C>T	XP_006715480.1:p.Leu8354=
XM_006715420.2:c.25048C>T	XP_006715483.1:p.Leu8350=
XM_006715421.2:c.25045C>T	XP_006715484.1:p.Leu8349=
XM_006715423.2:c.25201C>T	XP_006715486.1:p.Leu8401=
XM_006715424.2:c.25201C>T	XP_006715487.1:p.Leu8401=
XM_006715425.2:c.25132C>T	XP_006715488.1:p.Leu8378=
XM_011535641.2:c.25198C>T	XP_011533943.1:p.Leu8400=
XM_011535642.2:c.25186C>T	XP_011533944.1:p.Leu8396=
XM_011535645.2:c.22969C>T	XP_011533947.1:p.Leu7657=
XM_017010608.1:c.25201C>T	XP_016866097.1:p.Leu8401=
XM_017010609.1:c.25201C>T	XP_016866098.1:p.Leu8401=
XM_017010610.1:c.25180C>T	XP_016866099.1:p.Leu8394=
XM_017010611.2:c.25174C>T	XP_016866100.1:p.Leu8392=
XM_017010612.1:c.25123C>T	XP_016866101.1:p.Leu8375=
XM_017010613.1:c.25129C>T	XP_016866102.1:p.Leu8377=
XM_017010614.1:c.25045C>T	XP_016866103.1:p.Leu8349=
XM_017010615.1:c.24976C>T	XP_016866104.1:p.Leu8326=
XM_017010616.1:c.25132C>T	XP_016866105.1:p.Leu8378=
XM_017010617.1:c.25129C>T	XP_016866106.1:p.Leu8377=
XM_017010618.1:c.25117C>T	XP_016866107.1:p.Leu8373=
XM_017010619.1:c.23476C>T	XP_016866108.1:p.Leu7826=
NM_182961.4:c.25096C>T MANE Select	NP_892006.3:p.Leu8366=
NM_001347701.2:c.1702C>T	NP_001334630.1:p.Leu568=
NM_001347702.2:c.1630C>T MANE Plus Clinical	NP_001334631.1:p.Leu544=
NM_033071.5:c.24952C>T	NP_149062.2:p.Leu8318=