Canonical Allele Identifier: CA366118036

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152554989T>A (hg19) ; chr6:g.152233854T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152233854T>A , CM000668.2:g.152233854T>A	GRCh38
NC_000006.11:g.152554989T>A , CM000668.1:g.152554989T>A	GRCh37
NC_000006.10:g.152596682T>A	NCBI36
NG_012855.1:g.408546A>T
NG_012855.2:g.408546A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367255.10:c.20639A>T MANE Select	ENSP00000356224.5:p.Glu6880Val
ENST00000423061.6:c.20426A>T	ENSP00000396024.1:p.Glu6809Val
ENST00000341594.9:c.19424A>T	ENSP00000341887.6:p.Glu6475Val
ENST00000367255.9:c.20639A>T	ENSP00000356224.5:p.Glu6880Val
ENST00000367256.9:n.4331A>T
ENST00000409694.6:n.4223A>T
ENST00000423061.5:c.20426A>T	ENSP00000396024.1:p.Glu6809Val
NM_033071.3:c.20426A>T	NP_149062.1:p.Glu6809Val
NM_182961.3:c.20639A>T	NP_892006.3:p.Glu6880Val
XM_006715407.1:c.20675A>T	XP_006715470.1:p.Glu6892Val
XM_006715408.1:c.20663A>T	XP_006715471.1:p.Glu6888Val
XM_006715409.1:c.20654A>T	XP_006715472.1:p.Glu6885Val
XM_006715410.1:c.20675A>T	XP_006715473.1:p.Glu6892Val
XM_006715411.1:c.20624A>T	XP_006715474.1:p.Glu6875Val
XM_006715412.1:c.20660A>T	XP_006715475.1:p.Glu6887Val
XM_006715413.1:c.20675A>T	XP_006715476.1:p.Glu6892Val
XM_006715414.1:c.20603A>T	XP_006715477.1:p.Glu6868Val
XM_006715415.1:c.20675A>T	XP_006715478.1:p.Glu6892Val
XM_006715416.1:c.20660A>T	XP_006715479.1:p.Glu6887Val
XM_006715417.1:c.20534A>T	XP_006715480.1:p.Glu6845Val
XM_006715420.1:c.20522A>T	XP_006715483.1:p.Glu6841Val
XM_006715421.1:c.20519A>T	XP_006715484.1:p.Glu6840Val
XM_006715422.1:c.20516A>T	XP_006715485.1:p.Glu6839Val
XM_006715423.1:c.20675A>T	XP_006715486.1:p.Glu6892Val
XM_006715424.1:c.20675A>T	XP_006715487.1:p.Glu6892Val
XM_006715425.1:c.20675A>T	XP_006715488.1:p.Glu6892Val
XM_011535641.1:c.20672A>T	XP_011533943.1:p.Glu6891Val
XM_011535642.1:c.20660A>T	XP_011533944.1:p.Glu6887Val
XM_011535643.1:c.20510A>T	XP_011533945.1:p.Glu6837Val
XM_011535644.1:c.18950A>T	XP_011533946.1:p.Glu6317Val
XM_011535645.1:c.18443A>T	XP_011533947.1:p.Glu6148Val
XM_011535647.1:c.13910A>T	XP_011533949.1:p.Glu4637Val
XM_006715408.2:c.20663A>T	XP_006715471.1:p.Glu6888Val
XM_006715410.2:c.20675A>T	XP_006715473.1:p.Glu6892Val
XM_006715412.2:c.20660A>T	XP_006715475.1:p.Glu6887Val
XM_006715413.2:c.20675A>T	XP_006715476.1:p.Glu6892Val
XM_006715415.2:c.20675A>T	XP_006715478.1:p.Glu6892Val
XM_006715416.2:c.20660A>T	XP_006715479.1:p.Glu6887Val
XM_006715417.2:c.20534A>T	XP_006715480.1:p.Glu6845Val
XM_006715420.2:c.20522A>T	XP_006715483.1:p.Glu6841Val
XM_006715421.2:c.20519A>T	XP_006715484.1:p.Glu6840Val
XM_006715423.2:c.20675A>T	XP_006715486.1:p.Glu6892Val
XM_006715424.2:c.20675A>T	XP_006715487.1:p.Glu6892Val
XM_006715425.2:c.20675A>T	XP_006715488.1:p.Glu6892Val
XM_011535641.2:c.20672A>T	XP_011533943.1:p.Glu6891Val
XM_011535642.2:c.20660A>T	XP_011533944.1:p.Glu6887Val
XM_011535645.2:c.18443A>T	XP_011533947.1:p.Glu6148Val
XM_017010608.1:c.20675A>T	XP_016866097.1:p.Glu6892Val
XM_017010609.1:c.20675A>T	XP_016866098.1:p.Glu6892Val
XM_017010610.1:c.20654A>T	XP_016866099.1:p.Glu6885Val
XM_017010611.2:c.20648A>T	XP_016866100.1:p.Glu6883Val
XM_017010612.1:c.20597A>T	XP_016866101.1:p.Glu6866Val
XM_017010613.1:c.20672A>T	XP_016866102.1:p.Glu6891Val
XM_017010614.1:c.20519A>T	XP_016866103.1:p.Glu6840Val
XM_017010615.1:c.20519A>T	XP_016866104.1:p.Glu6840Val
XM_017010616.1:c.20675A>T	XP_016866105.1:p.Glu6892Val
XM_017010617.1:c.20672A>T	XP_016866106.1:p.Glu6891Val
XM_017010618.1:c.20660A>T	XP_016866107.1:p.Glu6887Val
XM_017010619.1:c.18950A>T	XP_016866108.1:p.Glu6317Val
NM_182961.4:c.20639A>T MANE Select	NP_892006.3:p.Glu6880Val
NM_033071.5:c.20426A>T	NP_149062.2:p.Glu6809Val