Canonical Allele Identifier: CA366089796

Gene: SYNE1

Linked Data

• COSMIC: COSM3777203 ; COSM3777204 ; COSM3777205 ; COSM3777206 ; COSM3777207
• MyVariant Identifiers: chr6:g.152583209C>G (hg19) ; chr6:g.152262074C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152262074C>G , CM000668.2:g.152262074C>G	GRCh38
NC_000006.11:g.152583209C>G , CM000668.1:g.152583209C>G	GRCh37
NC_000006.10:g.152624902C>G	NCBI36
NG_012855.1:g.380326G>C
NG_012855.2:g.380326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.18930G>C MANE Select	ENSP00000356224.5:p.Gln6310His
ENST00000423061.6:c.18717G>C	ENSP00000396024.1:p.Gln6239His
ENST00000341594.9:c.17715G>C	ENSP00000341887.6:p.Gln5905His
ENST00000367255.9:c.18930G>C	ENSP00000356224.5:p.Gln6310His
ENST00000367256.9:n.2622G>C
ENST00000409694.6:n.2514G>C
ENST00000423061.5:c.18717G>C	ENSP00000396024.1:p.Gln6239His
ENST00000545694.1:n.231G>C
NM_033071.3:c.18717G>C	NP_149062.1:p.Gln6239His
NM_182961.3:c.18930G>C	NP_892006.3:p.Gln6310His
XM_006715407.1:c.18966G>C	XP_006715470.1:p.Gln6322His
XM_006715408.1:c.18954G>C	XP_006715471.1:p.Gln6318His
XM_006715409.1:c.18945G>C	XP_006715472.1:p.Gln6315His
XM_006715410.1:c.18966G>C	XP_006715473.1:p.Gln6322His
XM_006715411.1:c.18915G>C	XP_006715474.1:p.Gln6305His
XM_006715412.1:c.18951G>C	XP_006715475.1:p.Gln6317His
XM_006715413.1:c.18966G>C	XP_006715476.1:p.Gln6322His
XM_006715414.1:c.18894G>C	XP_006715477.1:p.Gln6298His
XM_006715415.1:c.18966G>C	XP_006715478.1:p.Gln6322His
XM_006715416.1:c.18951G>C	XP_006715479.1:p.Gln6317His
XM_006715417.1:c.18825G>C	XP_006715480.1:p.Gln6275His
XM_006715420.1:c.18813G>C	XP_006715483.1:p.Gln6271His
XM_006715421.1:c.18810G>C	XP_006715484.1:p.Gln6270His
XM_006715422.1:c.18807G>C	XP_006715485.1:p.Gln6269His
XM_006715423.1:c.18966G>C	XP_006715486.1:p.Gln6322His
XM_006715424.1:c.18966G>C	XP_006715487.1:p.Gln6322His
XM_006715425.1:c.18966G>C	XP_006715488.1:p.Gln6322His
XM_011535641.1:c.18963G>C	XP_011533943.1:p.Gln6321His
XM_011535642.1:c.18951G>C	XP_011533944.1:p.Gln6317His
XM_011535643.1:c.18801G>C	XP_011533945.1:p.Gln6267His
XM_011535644.1:c.17241G>C	XP_011533946.1:p.Gln5747His
XM_011535645.1:c.16734G>C	XP_011533947.1:p.Gln5578His
XM_011535646.1:c.18966G>C	XP_011533948.1:p.Gln6322His
XM_011535647.1:c.12201G>C	XP_011533949.1:p.Gln4067His
XM_006715408.2:c.18954G>C	XP_006715471.1:p.Gln6318His
XM_006715410.2:c.18966G>C	XP_006715473.1:p.Gln6322His
XM_006715412.2:c.18951G>C	XP_006715475.1:p.Gln6317His
XM_006715413.2:c.18966G>C	XP_006715476.1:p.Gln6322His
XM_006715415.2:c.18966G>C	XP_006715478.1:p.Gln6322His
XM_006715416.2:c.18951G>C	XP_006715479.1:p.Gln6317His
XM_006715417.2:c.18825G>C	XP_006715480.1:p.Gln6275His
XM_006715420.2:c.18813G>C	XP_006715483.1:p.Gln6271His
XM_006715421.2:c.18810G>C	XP_006715484.1:p.Gln6270His
XM_006715423.2:c.18966G>C	XP_006715486.1:p.Gln6322His
XM_006715424.2:c.18966G>C	XP_006715487.1:p.Gln6322His
XM_006715425.2:c.18966G>C	XP_006715488.1:p.Gln6322His
XM_011535641.2:c.18963G>C	XP_011533943.1:p.Gln6321His
XM_011535642.2:c.18951G>C	XP_011533944.1:p.Gln6317His
XM_011535645.2:c.16734G>C	XP_011533947.1:p.Gln5578His
XM_017010608.1:c.18966G>C	XP_016866097.1:p.Gln6322His
XM_017010609.1:c.18966G>C	XP_016866098.1:p.Gln6322His
XM_017010610.1:c.18945G>C	XP_016866099.1:p.Gln6315His
XM_017010611.2:c.18939G>C	XP_016866100.1:p.Gln6313His
XM_017010612.1:c.18888G>C	XP_016866101.1:p.Gln6296His
XM_017010613.1:c.18963G>C	XP_016866102.1:p.Gln6321His
XM_017010614.1:c.18810G>C	XP_016866103.1:p.Gln6270His
XM_017010615.1:c.18810G>C	XP_016866104.1:p.Gln6270His
XM_017010616.1:c.18966G>C	XP_016866105.1:p.Gln6322His
XM_017010617.1:c.18963G>C	XP_016866106.1:p.Gln6321His
XM_017010618.1:c.18951G>C	XP_016866107.1:p.Gln6317His
XM_017010619.1:c.17241G>C	XP_016866108.1:p.Gln5747His
XR_001743287.1:n.19449G>C
NM_182961.4:c.18930G>C MANE Select	NP_892006.3:p.Gln6310His
NM_033071.5:c.18717G>C	NP_149062.2:p.Gln6239His