Canonical Allele Identifier: CA366099106

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152534779G>T (hg19) ; chr6:g.152213644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152213644G>T , CM000668.2:g.152213644G>T	GRCh38
NC_000006.11:g.152534779G>T , CM000668.1:g.152534779G>T	GRCh37
NC_000006.10:g.152576472G>T	NCBI36
NG_012855.1:g.428756C>A
NG_012855.2:g.428756C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367255.10:c.22462C>A MANE Select	ENSP00000356224.5:p.Gln7488Lys
ENST00000423061.6:c.22249C>A	ENSP00000396024.1:p.Gln7417Lys
ENST00000341594.9:c.21247C>A	ENSP00000341887.6:p.Gln7083Lys
ENST00000367251.7:c.1228C>A	ENSP00000356220.3:p.Gln410Lys
ENST00000367255.9:c.22462C>A	ENSP00000356224.5:p.Gln7488Lys
ENST00000367256.9:n.6154C>A
ENST00000367257.8:c.400C>A	ENSP00000356226.4:p.Gln134Lys
ENST00000409694.6:n.6046C>A
ENST00000423061.5:c.22249C>A	ENSP00000396024.1:p.Gln7417Lys
NM_033071.3:c.22249C>A	NP_149062.1:p.Gln7417Lys
NM_182961.3:c.22462C>A	NP_892006.3:p.Gln7488Lys
XM_006715407.1:c.22498C>A	XP_006715470.1:p.Gln7500Lys
XM_006715408.1:c.22486C>A	XP_006715471.1:p.Gln7496Lys
XM_006715409.1:c.22477C>A	XP_006715472.1:p.Gln7493Lys
XM_006715410.1:c.22498C>A	XP_006715473.1:p.Gln7500Lys
XM_006715411.1:c.22447C>A	XP_006715474.1:p.Gln7483Lys
XM_006715412.1:c.22483C>A	XP_006715475.1:p.Gln7495Lys
XM_006715413.1:c.22498C>A	XP_006715476.1:p.Gln7500Lys
XM_006715414.1:c.22426C>A	XP_006715477.1:p.Gln7476Lys
XM_006715415.1:c.22498C>A	XP_006715478.1:p.Gln7500Lys
XM_006715416.1:c.22483C>A	XP_006715479.1:p.Gln7495Lys
XM_006715417.1:c.22357C>A	XP_006715480.1:p.Gln7453Lys
XM_006715420.1:c.22345C>A	XP_006715483.1:p.Gln7449Lys
XM_006715421.1:c.22342C>A	XP_006715484.1:p.Gln7448Lys
XM_006715422.1:c.22339C>A	XP_006715485.1:p.Gln7447Lys
XM_006715423.1:c.22498C>A	XP_006715486.1:p.Gln7500Lys
XM_006715424.1:c.22498C>A	XP_006715487.1:p.Gln7500Lys
XM_006715425.1:c.22498C>A	XP_006715488.1:p.Gln7500Lys
XM_011535641.1:c.22495C>A	XP_011533943.1:p.Gln7499Lys
XM_011535642.1:c.22483C>A	XP_011533944.1:p.Gln7495Lys
XM_011535643.1:c.22333C>A	XP_011533945.1:p.Gln7445Lys
XM_011535644.1:c.20773C>A	XP_011533946.1:p.Gln6925Lys
XM_011535645.1:c.20266C>A	XP_011533947.1:p.Gln6756Lys
XM_011535647.1:c.15733C>A	XP_011533949.1:p.Gln5245Lys
XM_006715408.2:c.22486C>A	XP_006715471.1:p.Gln7496Lys
XM_006715410.2:c.22498C>A	XP_006715473.1:p.Gln7500Lys
XM_006715412.2:c.22483C>A	XP_006715475.1:p.Gln7495Lys
XM_006715413.2:c.22498C>A	XP_006715476.1:p.Gln7500Lys
XM_006715415.2:c.22498C>A	XP_006715478.1:p.Gln7500Lys
XM_006715416.2:c.22483C>A	XP_006715479.1:p.Gln7495Lys
XM_006715417.2:c.22357C>A	XP_006715480.1:p.Gln7453Lys
XM_006715420.2:c.22345C>A	XP_006715483.1:p.Gln7449Lys
XM_006715421.2:c.22342C>A	XP_006715484.1:p.Gln7448Lys
XM_006715423.2:c.22498C>A	XP_006715486.1:p.Gln7500Lys
XM_006715424.2:c.22498C>A	XP_006715487.1:p.Gln7500Lys
XM_006715425.2:c.22498C>A	XP_006715488.1:p.Gln7500Lys
XM_011535641.2:c.22495C>A	XP_011533943.1:p.Gln7499Lys
XM_011535642.2:c.22483C>A	XP_011533944.1:p.Gln7495Lys
XM_011535645.2:c.20266C>A	XP_011533947.1:p.Gln6756Lys
XM_017010608.1:c.22498C>A	XP_016866097.1:p.Gln7500Lys
XM_017010609.1:c.22498C>A	XP_016866098.1:p.Gln7500Lys
XM_017010610.1:c.22477C>A	XP_016866099.1:p.Gln7493Lys
XM_017010611.2:c.22471C>A	XP_016866100.1:p.Gln7491Lys
XM_017010612.1:c.22420C>A	XP_016866101.1:p.Gln7474Lys
XM_017010613.1:c.22495C>A	XP_016866102.1:p.Gln7499Lys
XM_017010614.1:c.22342C>A	XP_016866103.1:p.Gln7448Lys
XM_017010615.1:c.22342C>A	XP_016866104.1:p.Gln7448Lys
XM_017010616.1:c.22498C>A	XP_016866105.1:p.Gln7500Lys
XM_017010617.1:c.22495C>A	XP_016866106.1:p.Gln7499Lys
XM_017010618.1:c.22483C>A	XP_016866107.1:p.Gln7495Lys
XM_017010619.1:c.20773C>A	XP_016866108.1:p.Gln6925Lys
NM_182961.4:c.22462C>A MANE Select	NP_892006.3:p.Gln7488Lys
NM_033071.5:c.22249C>A	NP_149062.2:p.Gln7417Lys