Canonical Allele Identifier: CA366099501

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534866G>A (hg19) ; chr6:g.152213731G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213731G>A , CM000668.2:g.152213731G>A	GRCh38
NC_000006.11:g.152534866G>A , CM000668.1:g.152534866G>A	GRCh37
NC_000006.10:g.152576559G>A	NCBI36
NG_012855.1:g.428669C>T
NG_012855.2:g.428669C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22375C>T MANE Select	ENSP00000356224.5:p.Gln7459Ter
ENST00000423061.6:c.22162C>T	ENSP00000396024.1:p.Gln7388Ter
ENST00000341594.9:c.21160C>T	ENSP00000341887.6:p.Gln7054Ter
ENST00000367251.7:c.1141C>T	ENSP00000356220.3:p.Gln381Ter
ENST00000367255.9:c.22375C>T	ENSP00000356224.5:p.Gln7459Ter
ENST00000367256.9:n.6067C>T
ENST00000367257.8:c.313C>T	ENSP00000356226.4:p.Gln105Ter
ENST00000409694.6:n.5959C>T
ENST00000423061.5:c.22162C>T	ENSP00000396024.1:p.Gln7388Ter
NM_033071.3:c.22162C>T	NP_149062.1:p.Gln7388Ter
NM_182961.3:c.22375C>T	NP_892006.3:p.Gln7459Ter
XM_006715407.1:c.22411C>T	XP_006715470.1:p.Gln7471Ter
XM_006715408.1:c.22399C>T	XP_006715471.1:p.Gln7467Ter
XM_006715409.1:c.22390C>T	XP_006715472.1:p.Gln7464Ter
XM_006715410.1:c.22411C>T	XP_006715473.1:p.Gln7471Ter
XM_006715411.1:c.22360C>T	XP_006715474.1:p.Gln7454Ter
XM_006715412.1:c.22396C>T	XP_006715475.1:p.Gln7466Ter
XM_006715413.1:c.22411C>T	XP_006715476.1:p.Gln7471Ter
XM_006715414.1:c.22339C>T	XP_006715477.1:p.Gln7447Ter
XM_006715415.1:c.22411C>T	XP_006715478.1:p.Gln7471Ter
XM_006715416.1:c.22396C>T	XP_006715479.1:p.Gln7466Ter
XM_006715417.1:c.22270C>T	XP_006715480.1:p.Gln7424Ter
XM_006715420.1:c.22258C>T	XP_006715483.1:p.Gln7420Ter
XM_006715421.1:c.22255C>T	XP_006715484.1:p.Gln7419Ter
XM_006715422.1:c.22252C>T	XP_006715485.1:p.Gln7418Ter
XM_006715423.1:c.22411C>T	XP_006715486.1:p.Gln7471Ter
XM_006715424.1:c.22411C>T	XP_006715487.1:p.Gln7471Ter
XM_006715425.1:c.22411C>T	XP_006715488.1:p.Gln7471Ter
XM_011535641.1:c.22408C>T	XP_011533943.1:p.Gln7470Ter
XM_011535642.1:c.22396C>T	XP_011533944.1:p.Gln7466Ter
XM_011535643.1:c.22246C>T	XP_011533945.1:p.Gln7416Ter
XM_011535644.1:c.20686C>T	XP_011533946.1:p.Gln6896Ter
XM_011535645.1:c.20179C>T	XP_011533947.1:p.Gln6727Ter
XM_011535647.1:c.15646C>T	XP_011533949.1:p.Gln5216Ter
XM_006715408.2:c.22399C>T	XP_006715471.1:p.Gln7467Ter
XM_006715410.2:c.22411C>T	XP_006715473.1:p.Gln7471Ter
XM_006715412.2:c.22396C>T	XP_006715475.1:p.Gln7466Ter
XM_006715413.2:c.22411C>T	XP_006715476.1:p.Gln7471Ter
XM_006715415.2:c.22411C>T	XP_006715478.1:p.Gln7471Ter
XM_006715416.2:c.22396C>T	XP_006715479.1:p.Gln7466Ter
XM_006715417.2:c.22270C>T	XP_006715480.1:p.Gln7424Ter
XM_006715420.2:c.22258C>T	XP_006715483.1:p.Gln7420Ter
XM_006715421.2:c.22255C>T	XP_006715484.1:p.Gln7419Ter
XM_006715423.2:c.22411C>T	XP_006715486.1:p.Gln7471Ter
XM_006715424.2:c.22411C>T	XP_006715487.1:p.Gln7471Ter
XM_006715425.2:c.22411C>T	XP_006715488.1:p.Gln7471Ter
XM_011535641.2:c.22408C>T	XP_011533943.1:p.Gln7470Ter
XM_011535642.2:c.22396C>T	XP_011533944.1:p.Gln7466Ter
XM_011535645.2:c.20179C>T	XP_011533947.1:p.Gln6727Ter
XM_017010608.1:c.22411C>T	XP_016866097.1:p.Gln7471Ter
XM_017010609.1:c.22411C>T	XP_016866098.1:p.Gln7471Ter
XM_017010610.1:c.22390C>T	XP_016866099.1:p.Gln7464Ter
XM_017010611.2:c.22384C>T	XP_016866100.1:p.Gln7462Ter
XM_017010612.1:c.22333C>T	XP_016866101.1:p.Gln7445Ter
XM_017010613.1:c.22408C>T	XP_016866102.1:p.Gln7470Ter
XM_017010614.1:c.22255C>T	XP_016866103.1:p.Gln7419Ter
XM_017010615.1:c.22255C>T	XP_016866104.1:p.Gln7419Ter
XM_017010616.1:c.22411C>T	XP_016866105.1:p.Gln7471Ter
XM_017010617.1:c.22408C>T	XP_016866106.1:p.Gln7470Ter
XM_017010618.1:c.22396C>T	XP_016866107.1:p.Gln7466Ter
XM_017010619.1:c.20686C>T	XP_016866108.1:p.Gln6896Ter
NM_182961.4:c.22375C>T MANE Select	NP_892006.3:p.Gln7459Ter
NM_033071.5:c.22162C>T	NP_149062.2:p.Gln7388Ter