Canonical Allele Identifier: CA366099275

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534817G>A (hg19) ; chr6:g.152213682G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213682G>A , CM000668.2:g.152213682G>A	GRCh38
NC_000006.11:g.152534817G>A , CM000668.1:g.152534817G>A	GRCh37
NC_000006.10:g.152576510G>A	NCBI36
NG_012855.1:g.428718C>T
NG_012855.2:g.428718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22424C>T MANE Select	ENSP00000356224.5:p.Thr7475Ile
ENST00000423061.6:c.22211C>T	ENSP00000396024.1:p.Thr7404Ile
ENST00000341594.9:c.21209C>T	ENSP00000341887.6:p.Thr7070Ile
ENST00000367251.7:c.1190C>T	ENSP00000356220.3:p.Thr397Ile
ENST00000367255.9:c.22424C>T	ENSP00000356224.5:p.Thr7475Ile
ENST00000367256.9:n.6116C>T
ENST00000367257.8:c.362C>T	ENSP00000356226.4:p.Thr121Ile
ENST00000409694.6:n.6008C>T
ENST00000423061.5:c.22211C>T	ENSP00000396024.1:p.Thr7404Ile
NM_033071.3:c.22211C>T	NP_149062.1:p.Thr7404Ile
NM_182961.3:c.22424C>T	NP_892006.3:p.Thr7475Ile
XM_006715407.1:c.22460C>T	XP_006715470.1:p.Thr7487Ile
XM_006715408.1:c.22448C>T	XP_006715471.1:p.Thr7483Ile
XM_006715409.1:c.22439C>T	XP_006715472.1:p.Thr7480Ile
XM_006715410.1:c.22460C>T	XP_006715473.1:p.Thr7487Ile
XM_006715411.1:c.22409C>T	XP_006715474.1:p.Thr7470Ile
XM_006715412.1:c.22445C>T	XP_006715475.1:p.Thr7482Ile
XM_006715413.1:c.22460C>T	XP_006715476.1:p.Thr7487Ile
XM_006715414.1:c.22388C>T	XP_006715477.1:p.Thr7463Ile
XM_006715415.1:c.22460C>T	XP_006715478.1:p.Thr7487Ile
XM_006715416.1:c.22445C>T	XP_006715479.1:p.Thr7482Ile
XM_006715417.1:c.22319C>T	XP_006715480.1:p.Thr7440Ile
XM_006715420.1:c.22307C>T	XP_006715483.1:p.Thr7436Ile
XM_006715421.1:c.22304C>T	XP_006715484.1:p.Thr7435Ile
XM_006715422.1:c.22301C>T	XP_006715485.1:p.Thr7434Ile
XM_006715423.1:c.22460C>T	XP_006715486.1:p.Thr7487Ile
XM_006715424.1:c.22460C>T	XP_006715487.1:p.Thr7487Ile
XM_006715425.1:c.22460C>T	XP_006715488.1:p.Thr7487Ile
XM_011535641.1:c.22457C>T	XP_011533943.1:p.Thr7486Ile
XM_011535642.1:c.22445C>T	XP_011533944.1:p.Thr7482Ile
XM_011535643.1:c.22295C>T	XP_011533945.1:p.Thr7432Ile
XM_011535644.1:c.20735C>T	XP_011533946.1:p.Thr6912Ile
XM_011535645.1:c.20228C>T	XP_011533947.1:p.Thr6743Ile
XM_011535647.1:c.15695C>T	XP_011533949.1:p.Thr5232Ile
XM_006715408.2:c.22448C>T	XP_006715471.1:p.Thr7483Ile
XM_006715410.2:c.22460C>T	XP_006715473.1:p.Thr7487Ile
XM_006715412.2:c.22445C>T	XP_006715475.1:p.Thr7482Ile
XM_006715413.2:c.22460C>T	XP_006715476.1:p.Thr7487Ile
XM_006715415.2:c.22460C>T	XP_006715478.1:p.Thr7487Ile
XM_006715416.2:c.22445C>T	XP_006715479.1:p.Thr7482Ile
XM_006715417.2:c.22319C>T	XP_006715480.1:p.Thr7440Ile
XM_006715420.2:c.22307C>T	XP_006715483.1:p.Thr7436Ile
XM_006715421.2:c.22304C>T	XP_006715484.1:p.Thr7435Ile
XM_006715423.2:c.22460C>T	XP_006715486.1:p.Thr7487Ile
XM_006715424.2:c.22460C>T	XP_006715487.1:p.Thr7487Ile
XM_006715425.2:c.22460C>T	XP_006715488.1:p.Thr7487Ile
XM_011535641.2:c.22457C>T	XP_011533943.1:p.Thr7486Ile
XM_011535642.2:c.22445C>T	XP_011533944.1:p.Thr7482Ile
XM_011535645.2:c.20228C>T	XP_011533947.1:p.Thr6743Ile
XM_017010608.1:c.22460C>T	XP_016866097.1:p.Thr7487Ile
XM_017010609.1:c.22460C>T	XP_016866098.1:p.Thr7487Ile
XM_017010610.1:c.22439C>T	XP_016866099.1:p.Thr7480Ile
XM_017010611.2:c.22433C>T	XP_016866100.1:p.Thr7478Ile
XM_017010612.1:c.22382C>T	XP_016866101.1:p.Thr7461Ile
XM_017010613.1:c.22457C>T	XP_016866102.1:p.Thr7486Ile
XM_017010614.1:c.22304C>T	XP_016866103.1:p.Thr7435Ile
XM_017010615.1:c.22304C>T	XP_016866104.1:p.Thr7435Ile
XM_017010616.1:c.22460C>T	XP_016866105.1:p.Thr7487Ile
XM_017010617.1:c.22457C>T	XP_016866106.1:p.Thr7486Ile
XM_017010618.1:c.22445C>T	XP_016866107.1:p.Thr7482Ile
XM_017010619.1:c.20735C>T	XP_016866108.1:p.Thr6912Ile
NM_182961.4:c.22424C>T MANE Select	NP_892006.3:p.Thr7475Ile
NM_033071.5:c.22211C>T	NP_149062.2:p.Thr7404Ile