Canonical Allele Identifier: CA366080680
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152140100C>G , CM000668.2:g.152140100C>G GRCh38
NC_000006.11:g.152461235C>G , CM000668.1:g.152461235C>G GRCh37
NC_000006.10:g.152502928C>G NCBI36
NG_012855.1:g.502300G>C
NG_012855.2:g.502300G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1842G>C MANE Plus Clinical ENSP00000346701.4:p.Lys614Asn
ENST00000367255.10:c.25308G>C MANE Select ENSP00000356224.5:p.Lys8436Asn
ENST00000423061.6:c.25164G>C ENSP00000396024.1:p.Lys8388Asn
ENST00000672154.1:c.710G>C
ENST00000672169.1:c.1043G>C
ENST00000673173.1:c.952G>C
ENST00000673451.1:c.1080G>C ENSP00000500189.1:p.Lys360Asn
ENST00000341594.9:c.24093G>C ENSP00000341887.6:p.Lys8031Asn
ENST00000347037.9:n.2056G>C
ENST00000354674.4:c.1842G>C ENSP00000346701.4:p.Lys614Asn
ENST00000367251.7:c.4143G>C ENSP00000356220.3:p.Lys1381Asn
ENST00000367255.9:c.25308G>C ENSP00000356224.5:p.Lys8436Asn
ENST00000367256.9:n.9000G>C
ENST00000367257.8:c.3246G>C ENSP00000356226.4:p.Lys1082Asn
ENST00000409694.6:n.8892G>C
ENST00000423061.5:c.25164G>C ENSP00000396024.1:p.Lys8388Asn
ENST00000460912.6:n.1922G>C
ENST00000478916.5:n.4330G>C
ENST00000536990.5:n.2145G>C
ENST00000539504.5:c.1773G>C ENSP00000441052.1:p.Lys591Asn
NM_033071.3:c.25164G>C NP_149062.1:p.Lys8388Asn
NM_182961.3:c.25308G>C NP_892006.3:p.Lys8436Asn
XM_006715407.1:c.25413G>C XP_006715470.1:p.Lys8471Asn
XM_006715408.1:c.25401G>C XP_006715471.1:p.Lys8467Asn
XM_006715409.1:c.25392G>C XP_006715472.1:p.Lys8464Asn
XM_006715410.1:c.25413G>C XP_006715473.1:p.Lys8471Asn
XM_006715411.1:c.25362G>C XP_006715474.1:p.Lys8454Asn
XM_006715412.1:c.25398G>C XP_006715475.1:p.Lys8466Asn
XM_006715413.1:c.25344G>C XP_006715476.1:p.Lys8448Asn
XM_006715414.1:c.25341G>C XP_006715477.1:p.Lys8447Asn
XM_006715415.1:c.25344G>C XP_006715478.1:p.Lys8448Asn
XM_006715416.1:c.25329G>C XP_006715479.1:p.Lys8443Asn
XM_006715417.1:c.25272G>C XP_006715480.1:p.Lys8424Asn
XM_006715420.1:c.25260G>C XP_006715483.1:p.Lys8420Asn
XM_006715421.1:c.25257G>C XP_006715484.1:p.Lys8419Asn
XM_006715422.1:c.25254G>C XP_006715485.1:p.Lys8418Asn
XM_006715423.1:c.25413G>C XP_006715486.1:p.Lys8471Asn
XM_006715424.1:c.25413G>C XP_006715487.1:p.Lys8471Asn
XM_006715425.1:c.25344G>C XP_006715488.1:p.Lys8448Asn
XM_011535641.1:c.25410G>C XP_011533943.1:p.Lys8470Asn
XM_011535642.1:c.25398G>C XP_011533944.1:p.Lys8466Asn
XM_011535643.1:c.25248G>C XP_011533945.1:p.Lys8416Asn
XM_011535644.1:c.23688G>C XP_011533946.1:p.Lys7896Asn
XM_011535645.1:c.23181G>C XP_011533947.1:p.Lys7727Asn
XM_011535647.1:c.18648G>C XP_011533949.1:p.Lys6216Asn
NM_001347701.1:c.1914G>C NP_001334630.1:p.Lys638Asn
NM_001347702.1:c.1842G>C NP_001334631.1:p.Lys614Asn
XM_006715408.2:c.25401G>C XP_006715471.1:p.Lys8467Asn
XM_006715410.2:c.25413G>C XP_006715473.1:p.Lys8471Asn
XM_006715412.2:c.25398G>C XP_006715475.1:p.Lys8466Asn
XM_006715413.2:c.25344G>C XP_006715476.1:p.Lys8448Asn
XM_006715415.2:c.25344G>C XP_006715478.1:p.Lys8448Asn
XM_006715416.2:c.25329G>C XP_006715479.1:p.Lys8443Asn
XM_006715417.2:c.25272G>C XP_006715480.1:p.Lys8424Asn
XM_006715420.2:c.25260G>C XP_006715483.1:p.Lys8420Asn
XM_006715421.2:c.25257G>C XP_006715484.1:p.Lys8419Asn
XM_006715423.2:c.25413G>C XP_006715486.1:p.Lys8471Asn
XM_006715424.2:c.25413G>C XP_006715487.1:p.Lys8471Asn
XM_006715425.2:c.25344G>C XP_006715488.1:p.Lys8448Asn
XM_011535641.2:c.25410G>C XP_011533943.1:p.Lys8470Asn
XM_011535642.2:c.25398G>C XP_011533944.1:p.Lys8466Asn
XM_011535645.2:c.23181G>C XP_011533947.1:p.Lys7727Asn
XM_017010608.1:c.25413G>C XP_016866097.1:p.Lys8471Asn
XM_017010609.1:c.25413G>C XP_016866098.1:p.Lys8471Asn
XM_017010610.1:c.25392G>C XP_016866099.1:p.Lys8464Asn
XM_017010611.2:c.25386G>C XP_016866100.1:p.Lys8462Asn
XM_017010612.1:c.25335G>C XP_016866101.1:p.Lys8445Asn
XM_017010613.1:c.25341G>C XP_016866102.1:p.Lys8447Asn
XM_017010614.1:c.25257G>C XP_016866103.1:p.Lys8419Asn
XM_017010615.1:c.25188G>C XP_016866104.1:p.Lys8396Asn
XM_017010616.1:c.25344G>C XP_016866105.1:p.Lys8448Asn
XM_017010617.1:c.25341G>C XP_016866106.1:p.Lys8447Asn
XM_017010618.1:c.25329G>C XP_016866107.1:p.Lys8443Asn
XM_017010619.1:c.23688G>C XP_016866108.1:p.Lys7896Asn
NM_182961.4:c.25308G>C MANE Select NP_892006.3:p.Lys8436Asn
NM_001347701.2:c.1914G>C NP_001334630.1:p.Lys638Asn
NM_001347702.2:c.1842G>C MANE Plus Clinical NP_001334631.1:p.Lys614Asn
NM_033071.5:c.25164G>C NP_149062.2:p.Lys8388Asn