Canonical Allele Identifier: CA366081243

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152462346T>A (hg19) ; chr6:g.152141211T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152141211T>A , CM000668.2:g.152141211T>A	GRCh38
NC_000006.11:g.152462346T>A , CM000668.1:g.152462346T>A	GRCh37
NC_000006.10:g.152504039T>A	NCBI36
NG_012855.1:g.501189A>T
NG_012855.2:g.501189A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1772A>T MANE Plus Clinical	ENSP00000346701.4:p.Gln591Leu
ENST00000367255.10:c.25238A>T MANE Select	ENSP00000356224.5:p.Gln8413Leu
ENST00000423061.6:c.25094A>T	ENSP00000396024.1:p.Gln8365Leu
ENST00000672154.1:c.640A>T
ENST00000672169.1:c.973A>T
ENST00000673173.1:c.891-1050A>T
ENST00000673451.1:c.1010A>T	ENSP00000500189.1:p.Gln337Leu
ENST00000341594.9:c.24023A>T	ENSP00000341887.6:p.Gln8008Leu
ENST00000347037.9:n.1986A>T
ENST00000354674.4:c.1772A>T	ENSP00000346701.4:p.Gln591Leu
ENST00000367251.7:c.4073A>T	ENSP00000356220.3:p.Gln1358Leu
ENST00000367255.9:c.25238A>T	ENSP00000356224.5:p.Gln8413Leu
ENST00000367256.9:n.8930A>T
ENST00000367257.8:c.3176A>T	ENSP00000356226.4:p.Gln1059Leu
ENST00000409694.6:n.8822A>T
ENST00000423061.5:c.25094A>T	ENSP00000396024.1:p.Gln8365Leu
ENST00000460912.6:n.1852A>T
ENST00000478916.5:n.4260A>T
ENST00000536990.5:n.2075A>T
ENST00000539504.5:c.1703A>T	ENSP00000441052.1:p.Gln568Leu
NM_033071.3:c.25094A>T	NP_149062.1:p.Gln8365Leu
NM_182961.3:c.25238A>T	NP_892006.3:p.Gln8413Leu
XM_006715407.1:c.25343A>T	XP_006715470.1:p.Gln8448Leu
XM_006715408.1:c.25331A>T	XP_006715471.1:p.Gln8444Leu
XM_006715409.1:c.25322A>T	XP_006715472.1:p.Gln8441Leu
XM_006715410.1:c.25343A>T	XP_006715473.1:p.Gln8448Leu
XM_006715411.1:c.25292A>T	XP_006715474.1:p.Gln8431Leu
XM_006715412.1:c.25328A>T	XP_006715475.1:p.Gln8443Leu
XM_006715413.1:c.25274A>T	XP_006715476.1:p.Gln8425Leu
XM_006715414.1:c.25271A>T	XP_006715477.1:p.Gln8424Leu
XM_006715415.1:c.25274A>T	XP_006715478.1:p.Gln8425Leu
XM_006715416.1:c.25259A>T	XP_006715479.1:p.Gln8420Leu
XM_006715417.1:c.25202A>T	XP_006715480.1:p.Gln8401Leu
XM_006715420.1:c.25190A>T	XP_006715483.1:p.Gln8397Leu
XM_006715421.1:c.25187A>T	XP_006715484.1:p.Gln8396Leu
XM_006715422.1:c.25184A>T	XP_006715485.1:p.Gln8395Leu
XM_006715423.1:c.25343A>T	XP_006715486.1:p.Gln8448Leu
XM_006715424.1:c.25343A>T	XP_006715487.1:p.Gln8448Leu
XM_006715425.1:c.25274A>T	XP_006715488.1:p.Gln8425Leu
XM_011535641.1:c.25340A>T	XP_011533943.1:p.Gln8447Leu
XM_011535642.1:c.25328A>T	XP_011533944.1:p.Gln8443Leu
XM_011535643.1:c.25178A>T	XP_011533945.1:p.Gln8393Leu
XM_011535644.1:c.23618A>T	XP_011533946.1:p.Gln7873Leu
XM_011535645.1:c.23111A>T	XP_011533947.1:p.Gln7704Leu
XM_011535647.1:c.18578A>T	XP_011533949.1:p.Gln6193Leu
NM_001347701.1:c.1844A>T	NP_001334630.1:p.Gln615Leu
NM_001347702.1:c.1772A>T	NP_001334631.1:p.Gln591Leu
XM_006715408.2:c.25331A>T	XP_006715471.1:p.Gln8444Leu
XM_006715410.2:c.25343A>T	XP_006715473.1:p.Gln8448Leu
XM_006715412.2:c.25328A>T	XP_006715475.1:p.Gln8443Leu
XM_006715413.2:c.25274A>T	XP_006715476.1:p.Gln8425Leu
XM_006715415.2:c.25274A>T	XP_006715478.1:p.Gln8425Leu
XM_006715416.2:c.25259A>T	XP_006715479.1:p.Gln8420Leu
XM_006715417.2:c.25202A>T	XP_006715480.1:p.Gln8401Leu
XM_006715420.2:c.25190A>T	XP_006715483.1:p.Gln8397Leu
XM_006715421.2:c.25187A>T	XP_006715484.1:p.Gln8396Leu
XM_006715423.2:c.25343A>T	XP_006715486.1:p.Gln8448Leu
XM_006715424.2:c.25343A>T	XP_006715487.1:p.Gln8448Leu
XM_006715425.2:c.25274A>T	XP_006715488.1:p.Gln8425Leu
XM_011535641.2:c.25340A>T	XP_011533943.1:p.Gln8447Leu
XM_011535642.2:c.25328A>T	XP_011533944.1:p.Gln8443Leu
XM_011535645.2:c.23111A>T	XP_011533947.1:p.Gln7704Leu
XM_017010608.1:c.25343A>T	XP_016866097.1:p.Gln8448Leu
XM_017010609.1:c.25343A>T	XP_016866098.1:p.Gln8448Leu
XM_017010610.1:c.25322A>T	XP_016866099.1:p.Gln8441Leu
XM_017010611.2:c.25316A>T	XP_016866100.1:p.Gln8439Leu
XM_017010612.1:c.25265A>T	XP_016866101.1:p.Gln8422Leu
XM_017010613.1:c.25271A>T	XP_016866102.1:p.Gln8424Leu
XM_017010614.1:c.25187A>T	XP_016866103.1:p.Gln8396Leu
XM_017010615.1:c.25118A>T	XP_016866104.1:p.Gln8373Leu
XM_017010616.1:c.25274A>T	XP_016866105.1:p.Gln8425Leu
XM_017010617.1:c.25271A>T	XP_016866106.1:p.Gln8424Leu
XM_017010618.1:c.25259A>T	XP_016866107.1:p.Gln8420Leu
XM_017010619.1:c.23618A>T	XP_016866108.1:p.Gln7873Leu
NM_182961.4:c.25238A>T MANE Select	NP_892006.3:p.Gln8413Leu
NM_001347701.2:c.1844A>T	NP_001334630.1:p.Gln615Leu
NM_001347702.2:c.1772A>T MANE Plus Clinical	NP_001334631.1:p.Gln591Leu
NM_033071.5:c.25094A>T	NP_149062.2:p.Gln8365Leu