Canonical Allele Identifier: CA2841055735

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152151791dup , CM000668.2:g.152151791dup	GRCh38
NC_000006.11:g.152472926dup , CM000668.1:g.152472926dup	GRCh37
NC_000006.10:g.152514619dup	NCBI36
NG_012855.1:g.490612dup
NG_012855.2:g.490612dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.778-98dup MANE Plus Clinical	ENSP00000346701.4:n.778-98dup
ENST00000367255.10:c.24313-98dup MANE Select	ENSP00000356224.5:n.24313-98dup
ENST00000423061.6:c.24100-98dup	ENSP00000396024.1:n.24100-98dup
ENST00000672169.1:c.48-98dup
ENST00000673173.1:c.227-98dup
ENST00000673451.1:c.85-98dup	ENSP00000500189.1:n.85-98dup
ENST00000341594.9:c.23098-98dup	ENSP00000341887.6:n.23098-98dup
ENST00000347037.9:n.992-98dup
ENST00000354674.4:c.778-98dup	ENSP00000346701.4:n.778-98dup
ENST00000367251.7:c.3079-98dup	ENSP00000356220.3:n.3079-98dup
ENST00000367255.9:c.24313-98dup	ENSP00000356224.5:n.24313-98dup
ENST00000367256.9:n.8005-98dup
ENST00000367257.8:c.2251-98dup	ENSP00000356226.4:n.2251-98dup
ENST00000409694.6:n.7897-98dup
ENST00000423061.5:c.24100-98dup	ENSP00000396024.1:n.24100-98dup
ENST00000460912.6:n.858-98dup
ENST00000476519.1:n.375-98dup
ENST00000536990.5:n.1150-98dup
ENST00000539504.5:c.778-98dup	ENSP00000441052.1:n.778-98dup
NM_033071.3:c.24100-98dup	NP_149062.1:n.24100-98dup
NM_182961.3:c.24313-98dup	NP_892006.3:n.24313-98dup
XM_006715407.1:c.24349-98dup	XP_006715470.1:n.24349-98dup
XM_006715408.1:c.24337-98dup	XP_006715471.1:n.24337-98dup
XM_006715409.1:c.24328-98dup	XP_006715472.1:n.24328-98dup
XM_006715410.1:c.24349-98dup	XP_006715473.1:n.24349-98dup
XM_006715411.1:c.24298-98dup	XP_006715474.1:n.24298-98dup
XM_006715412.1:c.24334-98dup	XP_006715475.1:n.24334-98dup
XM_006715413.1:c.24349-98dup	XP_006715476.1:n.24349-98dup
XM_006715414.1:c.24277-98dup	XP_006715477.1:n.24277-98dup
XM_006715415.1:c.24349-98dup	XP_006715478.1:n.24349-98dup
XM_006715416.1:c.24334-98dup	XP_006715479.1:n.24334-98dup
XM_006715417.1:c.24208-98dup	XP_006715480.1:n.24208-98dup
XM_006715420.1:c.24196-98dup	XP_006715483.1:n.24196-98dup
XM_006715421.1:c.24193-98dup	XP_006715484.1:n.24193-98dup
XM_006715422.1:c.24190-98dup	XP_006715485.1:n.24190-98dup
XM_006715423.1:c.24349-98dup	XP_006715486.1:n.24349-98dup
XM_006715424.1:c.24349-98dup	XP_006715487.1:n.24349-98dup
XM_006715425.1:c.24349-98dup	XP_006715488.1:n.24349-98dup
XM_011535641.1:c.24346-98dup	XP_011533943.1:n.24346-98dup
XM_011535642.1:c.24334-98dup	XP_011533944.1:n.24334-98dup
XM_011535643.1:c.24184-98dup	XP_011533945.1:n.24184-98dup
XM_011535644.1:c.22624-98dup	XP_011533946.1:n.22624-98dup
XM_011535645.1:c.22117-98dup	XP_011533947.1:n.22117-98dup
XM_011535647.1:c.17584-98dup	XP_011533949.1:n.17584-98dup
NM_001347701.1:c.919-98dup	NP_001334630.1:n.919-98dup
NM_001347702.1:c.778-98dup	NP_001334631.1:n.778-98dup
XM_006715408.2:c.24337-98dup	XP_006715471.1:n.24337-98dup
XM_006715410.2:c.24349-98dup	XP_006715473.1:n.24349-98dup
XM_006715412.2:c.24334-98dup	XP_006715475.1:n.24334-98dup
XM_006715413.2:c.24349-98dup	XP_006715476.1:n.24349-98dup
XM_006715415.2:c.24349-98dup	XP_006715478.1:n.24349-98dup
XM_006715416.2:c.24334-98dup	XP_006715479.1:n.24334-98dup
XM_006715417.2:c.24208-98dup	XP_006715480.1:n.24208-98dup
XM_006715420.2:c.24196-98dup	XP_006715483.1:n.24196-98dup
XM_006715421.2:c.24193-98dup	XP_006715484.1:n.24193-98dup
XM_006715423.2:c.24349-98dup	XP_006715486.1:n.24349-98dup
XM_006715424.2:c.24349-98dup	XP_006715487.1:n.24349-98dup
XM_006715425.2:c.24349-98dup	XP_006715488.1:n.24349-98dup
XM_011535641.2:c.24346-98dup	XP_011533943.1:n.24346-98dup
XM_011535642.2:c.24334-98dup	XP_011533944.1:n.24334-98dup
XM_011535645.2:c.22117-98dup	XP_011533947.1:n.22117-98dup
XM_017010608.1:c.24349-98dup	XP_016866097.1:n.24349-98dup
XM_017010609.1:c.24349-98dup	XP_016866098.1:n.24349-98dup
XM_017010610.1:c.24328-98dup	XP_016866099.1:n.24328-98dup
XM_017010611.2:c.24322-98dup	XP_016866100.1:n.24322-98dup
XM_017010612.1:c.24271-98dup	XP_016866101.1:n.24271-98dup
XM_017010613.1:c.24346-98dup	XP_016866102.1:n.24346-98dup
XM_017010614.1:c.24193-98dup	XP_016866103.1:n.24193-98dup
XM_017010615.1:c.24193-98dup	XP_016866104.1:n.24193-98dup
XM_017010616.1:c.24349-98dup	XP_016866105.1:n.24349-98dup
XM_017010617.1:c.24346-98dup	XP_016866106.1:n.24346-98dup
XM_017010618.1:c.24334-98dup	XP_016866107.1:n.24334-98dup
XM_017010619.1:c.22624-98dup	XP_016866108.1:n.22624-98dup
NM_182961.4:c.24313-98dup MANE Select	NP_892006.3:n.24313-98dup
NM_001347701.2:c.919-98dup	NP_001334630.1:n.919-98dup
NM_001347702.2:c.778-98dup MANE Plus Clinical	NP_001334631.1:n.778-98dup
NM_033071.5:c.24100-98dup	NP_149062.2:n.24100-98dup