Canonical Allele Identifier: CA1673188737

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152122455T= , CM000668.2:g.152122455T= GRCh38
NC_000006.11:g.152443590T= , CM000668.1:g.152443590T= GRCh37
NC_000006.10:g.152485283T= NCBI36
NG_012855.1:g.519945A=
NG_008493.2:g.470765T=
NG_012855.2:g.519945A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.2909A= (SYNE1) MANE Plus Clinical ENSP00000346701.4:p.Asn970=
ENST00000367255.10:c.26375A= (SYNE1) MANE Select ENSP00000356224.5:p.Asn8792=
ENST00000423061.6:c.26231A= (SYNE1) ENSP00000396024.1:p.Asn8744=
ENST00000672154.1:c.1718A= (SYNE1)
ENST00000672169.1:c.2093A= (SYNE1)
ENST00000673173.1:c.1960A= (SYNE1)
ENST00000673451.1:c.2225A= (SYNE1) ENSP00000500189.1:n.2225A=
ENST00000341594.9:c.25160A= (SYNE1) ENSP00000341887.6:p.Asn8387=
ENST00000347037.9:n.3123A= (SYNE1)
ENST00000354674.4:c.2909A= (SYNE1) ENSP00000346701.4:p.Asn970=
ENST00000367251.7:c.5151A= (SYNE1) ENSP00000356220.3:n.5151A=
ENST00000367255.9:c.26375A= (SYNE1) ENSP00000356224.5:p.Asn8792=
ENST00000367256.9:n.10067A= (SYNE1)
ENST00000367257.8:c.4254A= (SYNE1) ENSP00000356226.4:n.4254A=
ENST00000409694.6:n.9959A= (SYNE1)
ENST00000423061.5:c.26231A= (SYNE1) ENSP00000396024.1:p.Asn8744=
ENST00000427531.6:c.851-2811T= (ESR1) ENSP00000394721.2:n.851-2811T=
ENST00000460912.6:n.2989A= (SYNE1)
ENST00000478916.5:n.7012A= (SYNE1)
ENST00000539504.5:c.2840A= (SYNE1) ENSP00000441052.1:p.Asn947=
NM_033071.3:c.26231A= (SYNE1) NP_149062.1:p.Asn8744=
NM_182961.3:c.26375A= (SYNE1) NP_892006.3:p.Asn8792=
XM_006715407.1:c.26522A= (SYNE1) XP_006715470.1:p.Asn8841=
XM_006715408.1:c.26510A= (SYNE1) XP_006715471.1:p.Asn8837=
XM_006715409.1:c.26501A= (SYNE1) XP_006715472.1:p.Asn8834=
XM_006715410.1:c.26480A= (SYNE1) XP_006715473.1:p.Asn8827=
XM_006715411.1:c.26471A= (SYNE1) XP_006715474.1:p.Asn8824=
XM_006715412.1:c.26465A= (SYNE1) XP_006715475.1:p.Asn8822=
XM_006715413.1:c.26453A= (SYNE1) XP_006715476.1:p.Asn8818=
XM_006715414.1:c.26450A= (SYNE1) XP_006715477.1:p.Asn8817=
XM_006715415.1:c.26411A= (SYNE1) XP_006715478.1:p.Asn8804=
XM_006715416.1:c.26396A= (SYNE1) XP_006715479.1:p.Asn8799=
XM_006715417.1:c.26381A= (SYNE1) XP_006715480.1:p.Asn8794=
XM_006715420.1:c.26369A= (SYNE1) XP_006715483.1:p.Asn8790=
XM_006715421.1:c.26366A= (SYNE1) XP_006715484.1:p.Asn8789=
XM_006715422.1:c.26363A= (SYNE1) XP_006715485.1:p.Asn8788=
XM_006715423.1:c.*186A= (SYNE1) XP_006715486.1:n.*186A=
XM_006715424.1:c.*186A= (SYNE1) XP_006715487.1:n.*186A=
XM_006715425.1:c.*186A= (SYNE1) XP_006715488.1:n.*186A=
XM_011535641.1:c.26519A= (SYNE1) XP_011533943.1:p.Asn8840=
XM_011535642.1:c.26507A= (SYNE1) XP_011533944.1:p.Asn8836=
XM_011535643.1:c.26357A= (SYNE1) XP_011533945.1:p.Asn8786=
XM_011535644.1:c.24797A= (SYNE1) XP_011533946.1:p.Asn8266=
XM_011535645.1:c.24290A= (SYNE1) XP_011533947.1:p.Asn8097=
XM_011535647.1:c.19757A= (SYNE1) XP_011533949.1:p.Asn6586=
NM_001328100.1:c.851-2811T= (ESR1) NP_001315029.1:n.851-2811T=
NM_001347701.1:c.*186A= (SYNE1) NP_001334630.1:n.*186A=
NM_001347702.1:c.2909A= (SYNE1) NP_001334631.1:p.Asn970=
XM_006715408.2:c.26510A= (SYNE1) XP_006715471.1:p.Asn8837=
XM_006715410.2:c.26480A= (SYNE1) XP_006715473.1:p.Asn8827=
XM_006715412.2:c.26465A= (SYNE1) XP_006715475.1:p.Asn8822=
XM_006715413.2:c.26453A= (SYNE1) XP_006715476.1:p.Asn8818=
XM_006715415.2:c.26411A= (SYNE1) XP_006715478.1:p.Asn8804=
XM_006715416.2:c.26396A= (SYNE1) XP_006715479.1:p.Asn8799=
XM_006715417.2:c.26381A= (SYNE1) XP_006715480.1:p.Asn8794=
XM_006715420.2:c.26369A= (SYNE1) XP_006715483.1:p.Asn8790=
XM_006715421.2:c.26366A= (SYNE1) XP_006715484.1:p.Asn8789=
XM_006715423.2:c.*186A= (SYNE1) XP_006715486.1:n.*186A=
XM_006715424.2:c.*186A= (SYNE1) XP_006715487.1:n.*186A=
XM_006715425.2:c.*186A= (SYNE1) XP_006715488.1:n.*186A=
XM_011535641.2:c.26519A= (SYNE1) XP_011533943.1:p.Asn8840=
XM_011535642.2:c.26507A= (SYNE1) XP_011533944.1:p.Asn8836=
XM_011535645.2:c.24290A= (SYNE1) XP_011533947.1:p.Asn8097=
XM_017010608.1:c.26522A= (SYNE1) XP_016866097.1:p.Asn8841=
XM_017010609.1:c.26522A= (SYNE1) XP_016866098.1:p.Asn8841=
XM_017010610.1:c.26501A= (SYNE1) XP_016866099.1:p.Asn8834=
XM_017010611.2:c.26495A= (SYNE1) XP_016866100.1:p.Asn8832=
XM_017010612.1:c.26444A= (SYNE1) XP_016866101.1:p.Asn8815=
XM_017010613.1:c.26408A= (SYNE1) XP_016866102.1:p.Asn8803=
XM_017010614.1:c.26366A= (SYNE1) XP_016866103.1:p.Asn8789=
XM_017010615.1:c.26255A= (SYNE1) XP_016866104.1:p.Asn8752=
XM_017010616.1:c.*186A= (SYNE1) XP_016866105.1:n.*186A=
XM_017010617.1:c.*186A= (SYNE1) XP_016866106.1:n.*186A=
XM_017010618.1:c.*186A= (SYNE1) XP_016866107.1:n.*186A=
XM_017010619.1:c.24797A= (SYNE1) XP_016866108.1:p.Asn8266=
NM_182961.4:c.26375A= (SYNE1) MANE Select NP_892006.3:p.Asn8792=
NM_001328100.2:c.851-2811T= (ESR1) NP_001315029.1:n.851-2811T=
NM_001347701.2:c.*186A= (SYNE1) NP_001334630.1:n.*186A=
NM_001347702.2:c.2909A= (SYNE1) MANE Plus Clinical NP_001334631.1:p.Asn970=
NM_033071.5:c.26231A= (SYNE1) NP_149062.2:p.Asn8744=