Canonical Allele Identifier: CA366080985

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461280C>G (hg19) ; chr6:g.152140145C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140145C>G , CM000668.2:g.152140145C>G	GRCh38
NC_000006.11:g.152461280C>G , CM000668.1:g.152461280C>G	GRCh37
NC_000006.10:g.152502973C>G	NCBI36
NG_012855.1:g.502255G>C
NG_012855.2:g.502255G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1797G>C MANE Plus Clinical	ENSP00000346701.4:p.Trp599Cys
ENST00000367255.10:c.25263G>C MANE Select	ENSP00000356224.5:p.Trp8421Cys
ENST00000423061.6:c.25119G>C	ENSP00000396024.1:p.Trp8373Cys
ENST00000672154.1:c.665G>C
ENST00000672169.1:c.998G>C
ENST00000673173.1:c.907G>C
ENST00000673451.1:c.1035G>C	ENSP00000500189.1:p.Trp345Cys
ENST00000341594.9:c.24048G>C	ENSP00000341887.6:p.Trp8016Cys
ENST00000347037.9:n.2011G>C
ENST00000354674.4:c.1797G>C	ENSP00000346701.4:p.Trp599Cys
ENST00000367251.7:c.4098G>C	ENSP00000356220.3:p.Trp1366Cys
ENST00000367255.9:c.25263G>C	ENSP00000356224.5:p.Trp8421Cys
ENST00000367256.9:n.8955G>C
ENST00000367257.8:c.3201G>C	ENSP00000356226.4:p.Trp1067Cys
ENST00000409694.6:n.8847G>C
ENST00000423061.5:c.25119G>C	ENSP00000396024.1:p.Trp8373Cys
ENST00000460912.6:n.1877G>C
ENST00000478916.5:n.4285G>C
ENST00000536990.5:n.2100G>C
ENST00000539504.5:c.1728G>C	ENSP00000441052.1:p.Trp576Cys
NM_033071.3:c.25119G>C	NP_149062.1:p.Trp8373Cys
NM_182961.3:c.25263G>C	NP_892006.3:p.Trp8421Cys
XM_006715407.1:c.25368G>C	XP_006715470.1:p.Trp8456Cys
XM_006715408.1:c.25356G>C	XP_006715471.1:p.Trp8452Cys
XM_006715409.1:c.25347G>C	XP_006715472.1:p.Trp8449Cys
XM_006715410.1:c.25368G>C	XP_006715473.1:p.Trp8456Cys
XM_006715411.1:c.25317G>C	XP_006715474.1:p.Trp8439Cys
XM_006715412.1:c.25353G>C	XP_006715475.1:p.Trp8451Cys
XM_006715413.1:c.25299G>C	XP_006715476.1:p.Trp8433Cys
XM_006715414.1:c.25296G>C	XP_006715477.1:p.Trp8432Cys
XM_006715415.1:c.25299G>C	XP_006715478.1:p.Trp8433Cys
XM_006715416.1:c.25284G>C	XP_006715479.1:p.Trp8428Cys
XM_006715417.1:c.25227G>C	XP_006715480.1:p.Trp8409Cys
XM_006715420.1:c.25215G>C	XP_006715483.1:p.Trp8405Cys
XM_006715421.1:c.25212G>C	XP_006715484.1:p.Trp8404Cys
XM_006715422.1:c.25209G>C	XP_006715485.1:p.Trp8403Cys
XM_006715423.1:c.25368G>C	XP_006715486.1:p.Trp8456Cys
XM_006715424.1:c.25368G>C	XP_006715487.1:p.Trp8456Cys
XM_006715425.1:c.25299G>C	XP_006715488.1:p.Trp8433Cys
XM_011535641.1:c.25365G>C	XP_011533943.1:p.Trp8455Cys
XM_011535642.1:c.25353G>C	XP_011533944.1:p.Trp8451Cys
XM_011535643.1:c.25203G>C	XP_011533945.1:p.Trp8401Cys
XM_011535644.1:c.23643G>C	XP_011533946.1:p.Trp7881Cys
XM_011535645.1:c.23136G>C	XP_011533947.1:p.Trp7712Cys
XM_011535647.1:c.18603G>C	XP_011533949.1:p.Trp6201Cys
NM_001347701.1:c.1869G>C	NP_001334630.1:p.Trp623Cys
NM_001347702.1:c.1797G>C	NP_001334631.1:p.Trp599Cys
XM_006715408.2:c.25356G>C	XP_006715471.1:p.Trp8452Cys
XM_006715410.2:c.25368G>C	XP_006715473.1:p.Trp8456Cys
XM_006715412.2:c.25353G>C	XP_006715475.1:p.Trp8451Cys
XM_006715413.2:c.25299G>C	XP_006715476.1:p.Trp8433Cys
XM_006715415.2:c.25299G>C	XP_006715478.1:p.Trp8433Cys
XM_006715416.2:c.25284G>C	XP_006715479.1:p.Trp8428Cys
XM_006715417.2:c.25227G>C	XP_006715480.1:p.Trp8409Cys
XM_006715420.2:c.25215G>C	XP_006715483.1:p.Trp8405Cys
XM_006715421.2:c.25212G>C	XP_006715484.1:p.Trp8404Cys
XM_006715423.2:c.25368G>C	XP_006715486.1:p.Trp8456Cys
XM_006715424.2:c.25368G>C	XP_006715487.1:p.Trp8456Cys
XM_006715425.2:c.25299G>C	XP_006715488.1:p.Trp8433Cys
XM_011535641.2:c.25365G>C	XP_011533943.1:p.Trp8455Cys
XM_011535642.2:c.25353G>C	XP_011533944.1:p.Trp8451Cys
XM_011535645.2:c.23136G>C	XP_011533947.1:p.Trp7712Cys
XM_017010608.1:c.25368G>C	XP_016866097.1:p.Trp8456Cys
XM_017010609.1:c.25368G>C	XP_016866098.1:p.Trp8456Cys
XM_017010610.1:c.25347G>C	XP_016866099.1:p.Trp8449Cys
XM_017010611.2:c.25341G>C	XP_016866100.1:p.Trp8447Cys
XM_017010612.1:c.25290G>C	XP_016866101.1:p.Trp8430Cys
XM_017010613.1:c.25296G>C	XP_016866102.1:p.Trp8432Cys
XM_017010614.1:c.25212G>C	XP_016866103.1:p.Trp8404Cys
XM_017010615.1:c.25143G>C	XP_016866104.1:p.Trp8381Cys
XM_017010616.1:c.25299G>C	XP_016866105.1:p.Trp8433Cys
XM_017010617.1:c.25296G>C	XP_016866106.1:p.Trp8432Cys
XM_017010618.1:c.25284G>C	XP_016866107.1:p.Trp8428Cys
XM_017010619.1:c.23643G>C	XP_016866108.1:p.Trp7881Cys
NM_182961.4:c.25263G>C MANE Select	NP_892006.3:p.Trp8421Cys
NM_001347701.2:c.1869G>C	NP_001334630.1:p.Trp623Cys
NM_001347702.2:c.1797G>C MANE Plus Clinical	NP_001334631.1:p.Trp599Cys
NM_033071.5:c.25119G>C	NP_149062.2:p.Trp8373Cys