Canonical Allele Identifier: CA1673241123

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213701T= , CM000668.2:g.152213701T=	GRCh38
NC_000006.11:g.152534836T= , CM000668.1:g.152534836T=	GRCh37
NC_000006.10:g.152576529T=	NCBI36
NG_012855.1:g.428699A=
NG_012855.2:g.428699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367255.10:c.22405A= MANE Select	ENSP00000356224.5:p.Met7469=
ENST00000423061.6:c.22192A=	ENSP00000396024.1:p.Met7398=
ENST00000341594.9:c.21190A=	ENSP00000341887.6:p.Met7064=
ENST00000367251.7:c.1171A=	ENSP00000356220.3:p.Met391=
ENST00000367255.9:c.22405A=	ENSP00000356224.5:p.Met7469=
ENST00000367256.9:n.6097A=
ENST00000367257.8:c.343A=	ENSP00000356226.4:p.Met115=
ENST00000409694.6:n.5989A=
ENST00000423061.5:c.22192A=	ENSP00000396024.1:p.Met7398=
NM_033071.3:c.22192A=	NP_149062.1:p.Met7398=
NM_182961.3:c.22405A=	NP_892006.3:p.Met7469=
XM_006715407.1:c.22441A=	XP_006715470.1:p.Met7481=
XM_006715408.1:c.22429A=	XP_006715471.1:p.Met7477=
XM_006715409.1:c.22420A=	XP_006715472.1:p.Met7474=
XM_006715410.1:c.22441A=	XP_006715473.1:p.Met7481=
XM_006715411.1:c.22390A=	XP_006715474.1:p.Met7464=
XM_006715412.1:c.22426A=	XP_006715475.1:p.Met7476=
XM_006715413.1:c.22441A=	XP_006715476.1:p.Met7481=
XM_006715414.1:c.22369A=	XP_006715477.1:p.Met7457=
XM_006715415.1:c.22441A=	XP_006715478.1:p.Met7481=
XM_006715416.1:c.22426A=	XP_006715479.1:p.Met7476=
XM_006715417.1:c.22300A=	XP_006715480.1:p.Met7434=
XM_006715420.1:c.22288A=	XP_006715483.1:p.Met7430=
XM_006715421.1:c.22285A=	XP_006715484.1:p.Met7429=
XM_006715422.1:c.22282A=	XP_006715485.1:p.Met7428=
XM_006715423.1:c.22441A=	XP_006715486.1:p.Met7481=
XM_006715424.1:c.22441A=	XP_006715487.1:p.Met7481=
XM_006715425.1:c.22441A=	XP_006715488.1:p.Met7481=
XM_011535641.1:c.22438A=	XP_011533943.1:p.Met7480=
XM_011535642.1:c.22426A=	XP_011533944.1:p.Met7476=
XM_011535643.1:c.22276A=	XP_011533945.1:p.Met7426=
XM_011535644.1:c.20716A=	XP_011533946.1:p.Met6906=
XM_011535645.1:c.20209A=	XP_011533947.1:p.Met6737=
XM_011535647.1:c.15676A=	XP_011533949.1:p.Met5226=
XM_006715408.2:c.22429A=	XP_006715471.1:p.Met7477=
XM_006715410.2:c.22441A=	XP_006715473.1:p.Met7481=
XM_006715412.2:c.22426A=	XP_006715475.1:p.Met7476=
XM_006715413.2:c.22441A=	XP_006715476.1:p.Met7481=
XM_006715415.2:c.22441A=	XP_006715478.1:p.Met7481=
XM_006715416.2:c.22426A=	XP_006715479.1:p.Met7476=
XM_006715417.2:c.22300A=	XP_006715480.1:p.Met7434=
XM_006715420.2:c.22288A=	XP_006715483.1:p.Met7430=
XM_006715421.2:c.22285A=	XP_006715484.1:p.Met7429=
XM_006715423.2:c.22441A=	XP_006715486.1:p.Met7481=
XM_006715424.2:c.22441A=	XP_006715487.1:p.Met7481=
XM_006715425.2:c.22441A=	XP_006715488.1:p.Met7481=
XM_011535641.2:c.22438A=	XP_011533943.1:p.Met7480=
XM_011535642.2:c.22426A=	XP_011533944.1:p.Met7476=
XM_011535645.2:c.20209A=	XP_011533947.1:p.Met6737=
XM_017010608.1:c.22441A=	XP_016866097.1:p.Met7481=
XM_017010609.1:c.22441A=	XP_016866098.1:p.Met7481=
XM_017010610.1:c.22420A=	XP_016866099.1:p.Met7474=
XM_017010611.2:c.22414A=	XP_016866100.1:p.Met7472=
XM_017010612.1:c.22363A=	XP_016866101.1:p.Met7455=
XM_017010613.1:c.22438A=	XP_016866102.1:p.Met7480=
XM_017010614.1:c.22285A=	XP_016866103.1:p.Met7429=
XM_017010615.1:c.22285A=	XP_016866104.1:p.Met7429=
XM_017010616.1:c.22441A=	XP_016866105.1:p.Met7481=
XM_017010617.1:c.22438A=	XP_016866106.1:p.Met7480=
XM_017010618.1:c.22426A=	XP_016866107.1:p.Met7476=
XM_017010619.1:c.20716A=	XP_016866108.1:p.Met6906=
NM_182961.4:c.22405A= MANE Select	NP_892006.3:p.Met7469=
NM_033071.5:c.22192A=	NP_149062.2:p.Met7398=