Canonical Allele Identifier: CA366103173

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152621783A>G (hg19) ; chr6:g.152300648A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152300648A>G , CM000668.2:g.152300648A>G	GRCh38
NC_000006.11:g.152621783A>G , CM000668.1:g.152621783A>G	GRCh37
NC_000006.10:g.152663476A>G	NCBI36
NG_012855.1:g.341752T>C
NG_012855.2:g.341752T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367255.10:c.17675T>C MANE Select	ENSP00000356224.5:p.Val5892Ala
ENST00000423061.6:c.17462T>C	ENSP00000396024.1:p.Val5821Ala
ENST00000341594.9:c.16460T>C	ENSP00000341887.6:p.Val5487Ala
ENST00000367255.9:c.17675T>C	ENSP00000356224.5:p.Val5892Ala
ENST00000367256.9:n.1367T>C
ENST00000409694.6:n.1259T>C
ENST00000423061.5:c.17462T>C	ENSP00000396024.1:p.Val5821Ala
ENST00000489156.1:n.401+1221T>C
ENST00000537033.1:c.341T>C	ENSP00000443879.1:p.Val114Ala
ENST00000540663.5:c.207+1221T>C	ENSP00000437411.1:n.207+1221T>C
NM_033071.3:c.17462T>C	NP_149062.1:p.Val5821Ala
NM_182961.3:c.17675T>C	NP_892006.3:p.Val5892Ala
XM_006715407.1:c.17696T>C	XP_006715470.1:p.Val5899Ala
XM_006715408.1:c.17696T>C	XP_006715471.1:p.Val5899Ala
XM_006715409.1:c.17675T>C	XP_006715472.1:p.Val5892Ala
XM_006715410.1:c.17696T>C	XP_006715473.1:p.Val5899Ala
XM_006715411.1:c.17645T>C	XP_006715474.1:p.Val5882Ala
XM_006715412.1:c.17696T>C	XP_006715475.1:p.Val5899Ala
XM_006715413.1:c.17696T>C	XP_006715476.1:p.Val5899Ala
XM_006715414.1:c.17624T>C	XP_006715477.1:p.Val5875Ala
XM_006715415.1:c.17696T>C	XP_006715478.1:p.Val5899Ala
XM_006715416.1:c.17696T>C	XP_006715479.1:p.Val5899Ala
XM_006715417.1:c.17562+1221T>C	XP_006715480.1:n.17562+1221T>C
XM_006715420.1:c.17562+1221T>C	XP_006715483.1:n.17562+1221T>C
XM_006715421.1:c.17540T>C	XP_006715484.1:p.Val5847Ala
XM_006715422.1:c.17537T>C	XP_006715485.1:p.Val5846Ala
XM_006715423.1:c.17696T>C	XP_006715486.1:p.Val5899Ala
XM_006715424.1:c.17696T>C	XP_006715487.1:p.Val5899Ala
XM_006715425.1:c.17696T>C	XP_006715488.1:p.Val5899Ala
XM_011535641.1:c.17696T>C	XP_011533943.1:p.Val5899Ala
XM_011535642.1:c.17696T>C	XP_011533944.1:p.Val5899Ala
XM_011535643.1:c.17531T>C	XP_011533945.1:p.Val5844Ala
XM_011535644.1:c.15971T>C	XP_011533946.1:p.Val5324Ala
XM_011535645.1:c.15464T>C	XP_011533947.1:p.Val5155Ala
XM_011535646.1:c.17696T>C	XP_011533948.1:p.Val5899Ala
XM_011535647.1:c.10931T>C	XP_011533949.1:p.Val3644Ala
XM_006715408.2:c.17696T>C	XP_006715471.1:p.Val5899Ala
XM_006715410.2:c.17696T>C	XP_006715473.1:p.Val5899Ala
XM_006715412.2:c.17696T>C	XP_006715475.1:p.Val5899Ala
XM_006715413.2:c.17696T>C	XP_006715476.1:p.Val5899Ala
XM_006715415.2:c.17696T>C	XP_006715478.1:p.Val5899Ala
XM_006715416.2:c.17696T>C	XP_006715479.1:p.Val5899Ala
XM_006715417.2:c.17562+1221T>C	XP_006715480.1:n.17562+1221T>C
XM_006715420.2:c.17562+1221T>C	XP_006715483.1:n.17562+1221T>C
XM_006715421.2:c.17540T>C	XP_006715484.1:p.Val5847Ala
XM_006715423.2:c.17696T>C	XP_006715486.1:p.Val5899Ala
XM_006715424.2:c.17696T>C	XP_006715487.1:p.Val5899Ala
XM_006715425.2:c.17696T>C	XP_006715488.1:p.Val5899Ala
XM_011535641.2:c.17696T>C	XP_011533943.1:p.Val5899Ala
XM_011535642.2:c.17696T>C	XP_011533944.1:p.Val5899Ala
XM_011535645.2:c.15464T>C	XP_011533947.1:p.Val5155Ala
XM_017010608.1:c.17696T>C	XP_016866097.1:p.Val5899Ala
XM_017010609.1:c.17696T>C	XP_016866098.1:p.Val5899Ala
XM_017010610.1:c.17675T>C	XP_016866099.1:p.Val5892Ala
XM_017010611.2:c.17669T>C	XP_016866100.1:p.Val5890Ala
XM_017010612.1:c.17618T>C	XP_016866101.1:p.Val5873Ala
XM_017010613.1:c.17696T>C	XP_016866102.1:p.Val5899Ala
XM_017010614.1:c.17562+1221T>C	XP_016866103.1:n.17562+1221T>C
XM_017010615.1:c.17562+1221T>C	XP_016866104.1:n.17562+1221T>C
XM_017010616.1:c.17696T>C	XP_016866105.1:p.Val5899Ala
XM_017010617.1:c.17696T>C	XP_016866106.1:p.Val5899Ala
XM_017010618.1:c.17696T>C	XP_016866107.1:p.Val5899Ala
XM_017010619.1:c.15971T>C	XP_016866108.1:p.Val5324Ala
XR_001743287.1:n.18179T>C
NM_182961.4:c.17675T>C MANE Select	NP_892006.3:p.Val5892Ala
NM_033071.5:c.17462T>C	NP_149062.2:p.Val5821Ala