Canonical Allele Identifier: CA452748228

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152473130C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152151995C>A , CM000668.2:g.152151995C>A	GRCh38
NC_000006.11:g.152473130C>A , CM000668.1:g.152473130C>A	GRCh37
NC_000006.10:g.152514823C>A	NCBI36
NG_012855.1:g.490405G>T
NG_012855.2:g.490405G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354674.5:c.741G>T MANE Plus Clinical	ENSP00000346701.4:p.Leu247=
ENST00000367255.10:c.24276G>T MANE Select	ENSP00000356224.5:p.Leu8092=
ENST00000423061.6:c.24063G>T	ENSP00000396024.1:p.Leu8021=
ENST00000672169.1:c.11G>T
ENST00000673173.1:c.190G>T
ENST00000673451.1:c.48G>T	ENSP00000500189.1:p.Leu16=
ENST00000341594.9:c.23061G>T	ENSP00000341887.6:p.Leu7687=
ENST00000347037.9:n.955G>T
ENST00000354674.4:c.741G>T	ENSP00000346701.4:p.Leu247=
ENST00000367251.7:c.3042G>T	ENSP00000356220.3:p.Leu1014=
ENST00000367255.9:c.24276G>T	ENSP00000356224.5:p.Leu8092=
ENST00000367256.9:n.7968G>T
ENST00000367257.8:c.2214G>T	ENSP00000356226.4:p.Leu738=
ENST00000409694.6:n.7860G>T
ENST00000423061.5:c.24063G>T	ENSP00000396024.1:p.Leu8021=
ENST00000460912.6:n.821G>T
ENST00000476519.1:n.338G>T
ENST00000536990.5:n.1113G>T
ENST00000539504.5:c.741G>T	ENSP00000441052.1:p.Leu247=
NM_033071.3:c.24063G>T	NP_149062.1:p.Leu8021=
NM_182961.3:c.24276G>T	NP_892006.3:p.Leu8092=
XM_006715407.1:c.24312G>T	XP_006715470.1:p.Leu8104=
XM_006715408.1:c.24300G>T	XP_006715471.1:p.Leu8100=
XM_006715409.1:c.24291G>T	XP_006715472.1:p.Leu8097=
XM_006715410.1:c.24312G>T	XP_006715473.1:p.Leu8104=
XM_006715411.1:c.24261G>T	XP_006715474.1:p.Leu8087=
XM_006715412.1:c.24297G>T	XP_006715475.1:p.Leu8099=
XM_006715413.1:c.24312G>T	XP_006715476.1:p.Leu8104=
XM_006715414.1:c.24240G>T	XP_006715477.1:p.Leu8080=
XM_006715415.1:c.24312G>T	XP_006715478.1:p.Leu8104=
XM_006715416.1:c.24297G>T	XP_006715479.1:p.Leu8099=
XM_006715417.1:c.24171G>T	XP_006715480.1:p.Leu8057=
XM_006715420.1:c.24159G>T	XP_006715483.1:p.Leu8053=
XM_006715421.1:c.24156G>T	XP_006715484.1:p.Leu8052=
XM_006715422.1:c.24153G>T	XP_006715485.1:p.Leu8051=
XM_006715423.1:c.24312G>T	XP_006715486.1:p.Leu8104=
XM_006715424.1:c.24312G>T	XP_006715487.1:p.Leu8104=
XM_006715425.1:c.24312G>T	XP_006715488.1:p.Leu8104=
XM_011535641.1:c.24309G>T	XP_011533943.1:p.Leu8103=
XM_011535642.1:c.24297G>T	XP_011533944.1:p.Leu8099=
XM_011535643.1:c.24147G>T	XP_011533945.1:p.Leu8049=
XM_011535644.1:c.22587G>T	XP_011533946.1:p.Leu7529=
XM_011535645.1:c.22080G>T	XP_011533947.1:p.Leu7360=
XM_011535647.1:c.17547G>T	XP_011533949.1:p.Leu5849=
NM_001347701.1:c.882G>T	NP_001334630.1:p.Leu294=
NM_001347702.1:c.741G>T	NP_001334631.1:p.Leu247=
XM_006715408.2:c.24300G>T	XP_006715471.1:p.Leu8100=
XM_006715410.2:c.24312G>T	XP_006715473.1:p.Leu8104=
XM_006715412.2:c.24297G>T	XP_006715475.1:p.Leu8099=
XM_006715413.2:c.24312G>T	XP_006715476.1:p.Leu8104=
XM_006715415.2:c.24312G>T	XP_006715478.1:p.Leu8104=
XM_006715416.2:c.24297G>T	XP_006715479.1:p.Leu8099=
XM_006715417.2:c.24171G>T	XP_006715480.1:p.Leu8057=
XM_006715420.2:c.24159G>T	XP_006715483.1:p.Leu8053=
XM_006715421.2:c.24156G>T	XP_006715484.1:p.Leu8052=
XM_006715423.2:c.24312G>T	XP_006715486.1:p.Leu8104=
XM_006715424.2:c.24312G>T	XP_006715487.1:p.Leu8104=
XM_006715425.2:c.24312G>T	XP_006715488.1:p.Leu8104=
XM_011535641.2:c.24309G>T	XP_011533943.1:p.Leu8103=
XM_011535642.2:c.24297G>T	XP_011533944.1:p.Leu8099=
XM_011535645.2:c.22080G>T	XP_011533947.1:p.Leu7360=
XM_017010608.1:c.24312G>T	XP_016866097.1:p.Leu8104=
XM_017010609.1:c.24312G>T	XP_016866098.1:p.Leu8104=
XM_017010610.1:c.24291G>T	XP_016866099.1:p.Leu8097=
XM_017010611.2:c.24285G>T	XP_016866100.1:p.Leu8095=
XM_017010612.1:c.24234G>T	XP_016866101.1:p.Leu8078=
XM_017010613.1:c.24309G>T	XP_016866102.1:p.Leu8103=
XM_017010614.1:c.24156G>T	XP_016866103.1:p.Leu8052=
XM_017010615.1:c.24156G>T	XP_016866104.1:p.Leu8052=
XM_017010616.1:c.24312G>T	XP_016866105.1:p.Leu8104=
XM_017010617.1:c.24309G>T	XP_016866106.1:p.Leu8103=
XM_017010618.1:c.24297G>T	XP_016866107.1:p.Leu8099=
XM_017010619.1:c.22587G>T	XP_016866108.1:p.Leu7529=
NM_182961.4:c.24276G>T MANE Select	NP_892006.3:p.Leu8092=
NM_001347701.2:c.882G>T	NP_001334630.1:p.Leu294=
NM_001347702.2:c.741G>T MANE Plus Clinical	NP_001334631.1:p.Leu247=
NM_033071.5:c.24063G>T	NP_149062.2:p.Leu8021=