Canonical Allele Identifier: CA366088449

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152122459T>A , CM000668.2:g.152122459T>A GRCh38
NC_000006.11:g.152443594T>A , CM000668.1:g.152443594T>A GRCh37
NC_000006.10:g.152485287T>A NCBI36
NG_012855.1:g.519941A>T
NG_008493.2:g.470769T>A
NG_012855.2:g.519941A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.2905A>T (SYNE1) MANE Plus Clinical ENSP00000346701.4:p.Thr969Ser
ENST00000367255.10:c.26371A>T (SYNE1) MANE Select ENSP00000356224.5:p.Thr8791Ser
ENST00000423061.6:c.26227A>T (SYNE1) ENSP00000396024.1:p.Thr8743Ser
ENST00000672154.1:c.1714A>T (SYNE1)
ENST00000672169.1:c.2089A>T (SYNE1)
ENST00000673173.1:c.1956A>T (SYNE1)
ENST00000673451.1:c.2221A>T (SYNE1) ENSP00000500189.1:n.2221A>T
ENST00000341594.9:c.25156A>T (SYNE1) ENSP00000341887.6:p.Thr8386Ser
ENST00000347037.9:n.3119A>T (SYNE1)
ENST00000354674.4:c.2905A>T (SYNE1) ENSP00000346701.4:p.Thr969Ser
ENST00000367251.7:c.5147A>T (SYNE1) ENSP00000356220.3:n.5147A>T
ENST00000367255.9:c.26371A>T (SYNE1) ENSP00000356224.5:p.Thr8791Ser
ENST00000367256.9:n.10063A>T (SYNE1)
ENST00000367257.8:c.4250A>T (SYNE1) ENSP00000356226.4:n.4250A>T
ENST00000409694.6:n.9955A>T (SYNE1)
ENST00000423061.5:c.26227A>T (SYNE1) ENSP00000396024.1:p.Thr8743Ser
ENST00000427531.6:c.851-2807T>A (ESR1) ENSP00000394721.2:n.851-2807T>A
ENST00000460912.6:n.2985A>T (SYNE1)
ENST00000478916.5:n.7008A>T (SYNE1)
ENST00000539504.5:c.2836A>T (SYNE1) ENSP00000441052.1:p.Thr946Ser
NM_033071.3:c.26227A>T (SYNE1) NP_149062.1:p.Thr8743Ser
NM_182961.3:c.26371A>T (SYNE1) NP_892006.3:p.Thr8791Ser
XM_006715407.1:c.26518A>T (SYNE1) XP_006715470.1:p.Thr8840Ser
XM_006715408.1:c.26506A>T (SYNE1) XP_006715471.1:p.Thr8836Ser
XM_006715409.1:c.26497A>T (SYNE1) XP_006715472.1:p.Thr8833Ser
XM_006715410.1:c.26476A>T (SYNE1) XP_006715473.1:p.Thr8826Ser
XM_006715411.1:c.26467A>T (SYNE1) XP_006715474.1:p.Thr8823Ser
XM_006715412.1:c.26461A>T (SYNE1) XP_006715475.1:p.Thr8821Ser
XM_006715413.1:c.26449A>T (SYNE1) XP_006715476.1:p.Thr8817Ser
XM_006715414.1:c.26446A>T (SYNE1) XP_006715477.1:p.Thr8816Ser
XM_006715415.1:c.26407A>T (SYNE1) XP_006715478.1:p.Thr8803Ser
XM_006715416.1:c.26392A>T (SYNE1) XP_006715479.1:p.Thr8798Ser
XM_006715417.1:c.26377A>T (SYNE1) XP_006715480.1:p.Thr8793Ser
XM_006715420.1:c.26365A>T (SYNE1) XP_006715483.1:p.Thr8789Ser
XM_006715421.1:c.26362A>T (SYNE1) XP_006715484.1:p.Thr8788Ser
XM_006715422.1:c.26359A>T (SYNE1) XP_006715485.1:p.Thr8787Ser
XM_006715423.1:c.*182A>T (SYNE1) XP_006715486.1:n.*182A>T
XM_006715424.1:c.*182A>T (SYNE1) XP_006715487.1:n.*182A>T
XM_006715425.1:c.*182A>T (SYNE1) XP_006715488.1:n.*182A>T
XM_011535641.1:c.26515A>T (SYNE1) XP_011533943.1:p.Thr8839Ser
XM_011535642.1:c.26503A>T (SYNE1) XP_011533944.1:p.Thr8835Ser
XM_011535643.1:c.26353A>T (SYNE1) XP_011533945.1:p.Thr8785Ser
XM_011535644.1:c.24793A>T (SYNE1) XP_011533946.1:p.Thr8265Ser
XM_011535645.1:c.24286A>T (SYNE1) XP_011533947.1:p.Thr8096Ser
XM_011535647.1:c.19753A>T (SYNE1) XP_011533949.1:p.Thr6585Ser
NM_001328100.1:c.851-2807T>A (ESR1) NP_001315029.1:n.851-2807T>A
NM_001347701.1:c.*182A>T (SYNE1) NP_001334630.1:n.*182A>T
NM_001347702.1:c.2905A>T (SYNE1) NP_001334631.1:p.Thr969Ser
XM_006715408.2:c.26506A>T (SYNE1) XP_006715471.1:p.Thr8836Ser
XM_006715410.2:c.26476A>T (SYNE1) XP_006715473.1:p.Thr8826Ser
XM_006715412.2:c.26461A>T (SYNE1) XP_006715475.1:p.Thr8821Ser
XM_006715413.2:c.26449A>T (SYNE1) XP_006715476.1:p.Thr8817Ser
XM_006715415.2:c.26407A>T (SYNE1) XP_006715478.1:p.Thr8803Ser
XM_006715416.2:c.26392A>T (SYNE1) XP_006715479.1:p.Thr8798Ser
XM_006715417.2:c.26377A>T (SYNE1) XP_006715480.1:p.Thr8793Ser
XM_006715420.2:c.26365A>T (SYNE1) XP_006715483.1:p.Thr8789Ser
XM_006715421.2:c.26362A>T (SYNE1) XP_006715484.1:p.Thr8788Ser
XM_006715423.2:c.*182A>T (SYNE1) XP_006715486.1:n.*182A>T
XM_006715424.2:c.*182A>T (SYNE1) XP_006715487.1:n.*182A>T
XM_006715425.2:c.*182A>T (SYNE1) XP_006715488.1:n.*182A>T
XM_011535641.2:c.26515A>T (SYNE1) XP_011533943.1:p.Thr8839Ser
XM_011535642.2:c.26503A>T (SYNE1) XP_011533944.1:p.Thr8835Ser
XM_011535645.2:c.24286A>T (SYNE1) XP_011533947.1:p.Thr8096Ser
XM_017010608.1:c.26518A>T (SYNE1) XP_016866097.1:p.Thr8840Ser
XM_017010609.1:c.26518A>T (SYNE1) XP_016866098.1:p.Thr8840Ser
XM_017010610.1:c.26497A>T (SYNE1) XP_016866099.1:p.Thr8833Ser
XM_017010611.2:c.26491A>T (SYNE1) XP_016866100.1:p.Thr8831Ser
XM_017010612.1:c.26440A>T (SYNE1) XP_016866101.1:p.Thr8814Ser
XM_017010613.1:c.26404A>T (SYNE1) XP_016866102.1:p.Thr8802Ser
XM_017010614.1:c.26362A>T (SYNE1) XP_016866103.1:p.Thr8788Ser
XM_017010615.1:c.26251A>T (SYNE1) XP_016866104.1:p.Thr8751Ser
XM_017010616.1:c.*182A>T (SYNE1) XP_016866105.1:n.*182A>T
XM_017010617.1:c.*182A>T (SYNE1) XP_016866106.1:n.*182A>T
XM_017010618.1:c.*182A>T (SYNE1) XP_016866107.1:n.*182A>T
XM_017010619.1:c.24793A>T (SYNE1) XP_016866108.1:p.Thr8265Ser
NM_182961.4:c.26371A>T (SYNE1) MANE Select NP_892006.3:p.Thr8791Ser
NM_001328100.2:c.851-2807T>A (ESR1) NP_001315029.1:n.851-2807T>A
NM_001347701.2:c.*182A>T (SYNE1) NP_001334630.1:n.*182A>T
NM_001347702.2:c.2905A>T (SYNE1) MANE Plus Clinical NP_001334631.1:p.Thr969Ser
NM_033071.5:c.26227A>T (SYNE1) NP_149062.2:p.Thr8743Ser