Canonical Allele Identifier: CA366082948

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152464775T>G (hg19) ; chr6:g.152143640T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152143640T>G , CM000668.2:g.152143640T>G	GRCh38
NC_000006.11:g.152464775T>G , CM000668.1:g.152464775T>G	GRCh37
NC_000006.10:g.152506468T>G	NCBI36
NG_012855.1:g.498760A>C
NG_012855.2:g.498760A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1636A>C MANE Plus Clinical	ENSP00000346701.4:p.Thr546Pro
ENST00000367255.10:c.25102A>C MANE Select	ENSP00000356224.5:p.Thr8368Pro
ENST00000423061.6:c.24958A>C	ENSP00000396024.1:p.Thr8320Pro
ENST00000672154.1:c.504A>C
ENST00000672169.1:c.837A>C
ENST00000673173.1:c.891-3479A>C
ENST00000673451.1:c.874A>C	ENSP00000500189.1:p.Thr292Pro
ENST00000341594.9:c.23887A>C	ENSP00000341887.6:p.Thr7963Pro
ENST00000347037.9:n.1850A>C
ENST00000354674.4:c.1636A>C	ENSP00000346701.4:p.Thr546Pro
ENST00000367251.7:c.3937A>C	ENSP00000356220.3:p.Thr1313Pro
ENST00000367255.9:c.25102A>C	ENSP00000356224.5:p.Thr8368Pro
ENST00000367256.9:n.8794A>C
ENST00000367257.8:c.3040A>C	ENSP00000356226.4:p.Thr1014Pro
ENST00000409694.6:n.8686A>C
ENST00000423061.5:c.24958A>C	ENSP00000396024.1:p.Thr8320Pro
ENST00000460912.6:n.1716A>C
ENST00000478916.5:n.4124A>C
ENST00000536990.5:n.1939A>C
ENST00000539504.5:c.1567A>C	ENSP00000441052.1:p.Thr523Pro
NM_033071.3:c.24958A>C	NP_149062.1:p.Thr8320Pro
NM_182961.3:c.25102A>C	NP_892006.3:p.Thr8368Pro
XM_006715407.1:c.25207A>C	XP_006715470.1:p.Thr8403Pro
XM_006715408.1:c.25195A>C	XP_006715471.1:p.Thr8399Pro
XM_006715409.1:c.25186A>C	XP_006715472.1:p.Thr8396Pro
XM_006715410.1:c.25207A>C	XP_006715473.1:p.Thr8403Pro
XM_006715411.1:c.25156A>C	XP_006715474.1:p.Thr8386Pro
XM_006715412.1:c.25192A>C	XP_006715475.1:p.Thr8398Pro
XM_006715413.1:c.25138A>C	XP_006715476.1:p.Thr8380Pro
XM_006715414.1:c.25135A>C	XP_006715477.1:p.Thr8379Pro
XM_006715415.1:c.25138A>C	XP_006715478.1:p.Thr8380Pro
XM_006715416.1:c.25123A>C	XP_006715479.1:p.Thr8375Pro
XM_006715417.1:c.25066A>C	XP_006715480.1:p.Thr8356Pro
XM_006715420.1:c.25054A>C	XP_006715483.1:p.Thr8352Pro
XM_006715421.1:c.25051A>C	XP_006715484.1:p.Thr8351Pro
XM_006715422.1:c.25048A>C	XP_006715485.1:p.Thr8350Pro
XM_006715423.1:c.25207A>C	XP_006715486.1:p.Thr8403Pro
XM_006715424.1:c.25207A>C	XP_006715487.1:p.Thr8403Pro
XM_006715425.1:c.25138A>C	XP_006715488.1:p.Thr8380Pro
XM_011535641.1:c.25204A>C	XP_011533943.1:p.Thr8402Pro
XM_011535642.1:c.25192A>C	XP_011533944.1:p.Thr8398Pro
XM_011535643.1:c.25042A>C	XP_011533945.1:p.Thr8348Pro
XM_011535644.1:c.23482A>C	XP_011533946.1:p.Thr7828Pro
XM_011535645.1:c.22975A>C	XP_011533947.1:p.Thr7659Pro
XM_011535647.1:c.18442A>C	XP_011533949.1:p.Thr6148Pro
NM_001347701.1:c.1708A>C	NP_001334630.1:p.Thr570Pro
NM_001347702.1:c.1636A>C	NP_001334631.1:p.Thr546Pro
XM_006715408.2:c.25195A>C	XP_006715471.1:p.Thr8399Pro
XM_006715410.2:c.25207A>C	XP_006715473.1:p.Thr8403Pro
XM_006715412.2:c.25192A>C	XP_006715475.1:p.Thr8398Pro
XM_006715413.2:c.25138A>C	XP_006715476.1:p.Thr8380Pro
XM_006715415.2:c.25138A>C	XP_006715478.1:p.Thr8380Pro
XM_006715416.2:c.25123A>C	XP_006715479.1:p.Thr8375Pro
XM_006715417.2:c.25066A>C	XP_006715480.1:p.Thr8356Pro
XM_006715420.2:c.25054A>C	XP_006715483.1:p.Thr8352Pro
XM_006715421.2:c.25051A>C	XP_006715484.1:p.Thr8351Pro
XM_006715423.2:c.25207A>C	XP_006715486.1:p.Thr8403Pro
XM_006715424.2:c.25207A>C	XP_006715487.1:p.Thr8403Pro
XM_006715425.2:c.25138A>C	XP_006715488.1:p.Thr8380Pro
XM_011535641.2:c.25204A>C	XP_011533943.1:p.Thr8402Pro
XM_011535642.2:c.25192A>C	XP_011533944.1:p.Thr8398Pro
XM_011535645.2:c.22975A>C	XP_011533947.1:p.Thr7659Pro
XM_017010608.1:c.25207A>C	XP_016866097.1:p.Thr8403Pro
XM_017010609.1:c.25207A>C	XP_016866098.1:p.Thr8403Pro
XM_017010610.1:c.25186A>C	XP_016866099.1:p.Thr8396Pro
XM_017010611.2:c.25180A>C	XP_016866100.1:p.Thr8394Pro
XM_017010612.1:c.25129A>C	XP_016866101.1:p.Thr8377Pro
XM_017010613.1:c.25135A>C	XP_016866102.1:p.Thr8379Pro
XM_017010614.1:c.25051A>C	XP_016866103.1:p.Thr8351Pro
XM_017010615.1:c.24982A>C	XP_016866104.1:p.Thr8328Pro
XM_017010616.1:c.25138A>C	XP_016866105.1:p.Thr8380Pro
XM_017010617.1:c.25135A>C	XP_016866106.1:p.Thr8379Pro
XM_017010618.1:c.25123A>C	XP_016866107.1:p.Thr8375Pro
XM_017010619.1:c.23482A>C	XP_016866108.1:p.Thr7828Pro
NM_182961.4:c.25102A>C MANE Select	NP_892006.3:p.Thr8368Pro
NM_001347701.2:c.1708A>C	NP_001334630.1:p.Thr570Pro
NM_001347702.2:c.1636A>C MANE Plus Clinical	NP_001334631.1:p.Thr546Pro
NM_033071.5:c.24958A>C	NP_149062.2:p.Thr8320Pro