Canonical Allele Identifier: CA366079946
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152139958T>G , CM000668.2:g.152139958T>G GRCh38
NC_000006.11:g.152461093T>G , CM000668.1:g.152461093T>G GRCh37
NC_000006.10:g.152502786T>G NCBI36
NG_012855.1:g.502442A>C
NG_012855.2:g.502442A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354674.5:c.1984A>C MANE Plus Clinical ENSP00000346701.4:p.Lys662Gln
ENST00000367255.10:c.25450A>C MANE Select ENSP00000356224.5:p.Lys8484Gln
ENST00000423061.6:c.25306A>C ENSP00000396024.1:p.Lys8436Gln
ENST00000672154.1:c.852A>C
ENST00000672169.1:c.1185A>C
ENST00000673173.1:c.1094A>C
ENST00000673451.1:c.1222A>C ENSP00000500189.1:p.Lys408Gln
ENST00000341594.9:c.24235A>C ENSP00000341887.6:p.Lys8079Gln
ENST00000347037.9:n.2198A>C
ENST00000354674.4:c.1984A>C ENSP00000346701.4:p.Lys662Gln
ENST00000367251.7:c.4285A>C ENSP00000356220.3:p.Lys1429Gln
ENST00000367255.9:c.25450A>C ENSP00000356224.5:p.Lys8484Gln
ENST00000367256.9:n.9142A>C
ENST00000367257.8:c.3388A>C ENSP00000356226.4:p.Lys1130Gln
ENST00000409694.6:n.9034A>C
ENST00000423061.5:c.25306A>C ENSP00000396024.1:p.Lys8436Gln
ENST00000460912.6:n.2064A>C
ENST00000478916.5:n.4472A>C
ENST00000536990.5:n.2287A>C
ENST00000539504.5:c.1915A>C ENSP00000441052.1:p.Lys639Gln
NM_033071.3:c.25306A>C NP_149062.1:p.Lys8436Gln
NM_182961.3:c.25450A>C NP_892006.3:p.Lys8484Gln
XM_006715407.1:c.25555A>C XP_006715470.1:p.Lys8519Gln
XM_006715408.1:c.25543A>C XP_006715471.1:p.Lys8515Gln
XM_006715409.1:c.25534A>C XP_006715472.1:p.Lys8512Gln
XM_006715410.1:c.25555A>C XP_006715473.1:p.Lys8519Gln
XM_006715411.1:c.25504A>C XP_006715474.1:p.Lys8502Gln
XM_006715412.1:c.25540A>C XP_006715475.1:p.Lys8514Gln
XM_006715413.1:c.25486A>C XP_006715476.1:p.Lys8496Gln
XM_006715414.1:c.25483A>C XP_006715477.1:p.Lys8495Gln
XM_006715415.1:c.25486A>C XP_006715478.1:p.Lys8496Gln
XM_006715416.1:c.25471A>C XP_006715479.1:p.Lys8491Gln
XM_006715417.1:c.25414A>C XP_006715480.1:p.Lys8472Gln
XM_006715420.1:c.25402A>C XP_006715483.1:p.Lys8468Gln
XM_006715421.1:c.25399A>C XP_006715484.1:p.Lys8467Gln
XM_006715422.1:c.25396A>C XP_006715485.1:p.Lys8466Gln
XM_006715423.1:c.25555A>C XP_006715486.1:p.Lys8519Gln
XM_006715424.1:c.25555A>C XP_006715487.1:p.Lys8519Gln
XM_006715425.1:c.25486A>C XP_006715488.1:p.Lys8496Gln
XM_011535641.1:c.25552A>C XP_011533943.1:p.Lys8518Gln
XM_011535642.1:c.25540A>C XP_011533944.1:p.Lys8514Gln
XM_011535643.1:c.25390A>C XP_011533945.1:p.Lys8464Gln
XM_011535644.1:c.23830A>C XP_011533946.1:p.Lys7944Gln
XM_011535645.1:c.23323A>C XP_011533947.1:p.Lys7775Gln
XM_011535647.1:c.18790A>C XP_011533949.1:p.Lys6264Gln
NM_001347701.1:c.2056A>C NP_001334630.1:p.Lys686Gln
NM_001347702.1:c.1984A>C NP_001334631.1:p.Lys662Gln
XM_006715408.2:c.25543A>C XP_006715471.1:p.Lys8515Gln
XM_006715410.2:c.25555A>C XP_006715473.1:p.Lys8519Gln
XM_006715412.2:c.25540A>C XP_006715475.1:p.Lys8514Gln
XM_006715413.2:c.25486A>C XP_006715476.1:p.Lys8496Gln
XM_006715415.2:c.25486A>C XP_006715478.1:p.Lys8496Gln
XM_006715416.2:c.25471A>C XP_006715479.1:p.Lys8491Gln
XM_006715417.2:c.25414A>C XP_006715480.1:p.Lys8472Gln
XM_006715420.2:c.25402A>C XP_006715483.1:p.Lys8468Gln
XM_006715421.2:c.25399A>C XP_006715484.1:p.Lys8467Gln
XM_006715423.2:c.25555A>C XP_006715486.1:p.Lys8519Gln
XM_006715424.2:c.25555A>C XP_006715487.1:p.Lys8519Gln
XM_006715425.2:c.25486A>C XP_006715488.1:p.Lys8496Gln
XM_011535641.2:c.25552A>C XP_011533943.1:p.Lys8518Gln
XM_011535642.2:c.25540A>C XP_011533944.1:p.Lys8514Gln
XM_011535645.2:c.23323A>C XP_011533947.1:p.Lys7775Gln
XM_017010608.1:c.25555A>C XP_016866097.1:p.Lys8519Gln
XM_017010609.1:c.25555A>C XP_016866098.1:p.Lys8519Gln
XM_017010610.1:c.25534A>C XP_016866099.1:p.Lys8512Gln
XM_017010611.2:c.25528A>C XP_016866100.1:p.Lys8510Gln
XM_017010612.1:c.25477A>C XP_016866101.1:p.Lys8493Gln
XM_017010613.1:c.25483A>C XP_016866102.1:p.Lys8495Gln
XM_017010614.1:c.25399A>C XP_016866103.1:p.Lys8467Gln
XM_017010615.1:c.25330A>C XP_016866104.1:p.Lys8444Gln
XM_017010616.1:c.25486A>C XP_016866105.1:p.Lys8496Gln
XM_017010617.1:c.25483A>C XP_016866106.1:p.Lys8495Gln
XM_017010618.1:c.25471A>C XP_016866107.1:p.Lys8491Gln
XM_017010619.1:c.23830A>C XP_016866108.1:p.Lys7944Gln
NM_182961.4:c.25450A>C MANE Select NP_892006.3:p.Lys8484Gln
NM_001347701.2:c.2056A>C NP_001334630.1:p.Lys686Gln
NM_001347702.2:c.1984A>C MANE Plus Clinical NP_001334631.1:p.Lys662Gln
NM_033071.5:c.25306A>C NP_149062.2:p.Lys8436Gln