Canonical Allele Identifier: CA366080549
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152140081G>T , CM000668.2:g.152140081G>T GRCh38
NC_000006.11:g.152461216G>T , CM000668.1:g.152461216G>T GRCh37
NC_000006.10:g.152502909G>T NCBI36
NG_012855.1:g.502319C>A
NG_012855.2:g.502319C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1861C>A MANE Plus Clinical ENSP00000346701.4:p.Gln621Lys
ENST00000367255.10:c.25327C>A MANE Select ENSP00000356224.5:p.Gln8443Lys
ENST00000423061.6:c.25183C>A ENSP00000396024.1:p.Gln8395Lys
ENST00000672154.1:c.729C>A
ENST00000672169.1:c.1062C>A
ENST00000673173.1:c.971C>A
ENST00000673451.1:c.1099C>A ENSP00000500189.1:p.Gln367Lys
ENST00000341594.9:c.24112C>A ENSP00000341887.6:p.Gln8038Lys
ENST00000347037.9:n.2075C>A
ENST00000354674.4:c.1861C>A ENSP00000346701.4:p.Gln621Lys
ENST00000367251.7:c.4162C>A ENSP00000356220.3:p.Gln1388Lys
ENST00000367255.9:c.25327C>A ENSP00000356224.5:p.Gln8443Lys
ENST00000367256.9:n.9019C>A
ENST00000367257.8:c.3265C>A ENSP00000356226.4:p.Gln1089Lys
ENST00000409694.6:n.8911C>A
ENST00000423061.5:c.25183C>A ENSP00000396024.1:p.Gln8395Lys
ENST00000460912.6:n.1941C>A
ENST00000478916.5:n.4349C>A
ENST00000536990.5:n.2164C>A
ENST00000539504.5:c.1792C>A ENSP00000441052.1:p.Gln598Lys
NM_033071.3:c.25183C>A NP_149062.1:p.Gln8395Lys
NM_182961.3:c.25327C>A NP_892006.3:p.Gln8443Lys
XM_006715407.1:c.25432C>A XP_006715470.1:p.Gln8478Lys
XM_006715408.1:c.25420C>A XP_006715471.1:p.Gln8474Lys
XM_006715409.1:c.25411C>A XP_006715472.1:p.Gln8471Lys
XM_006715410.1:c.25432C>A XP_006715473.1:p.Gln8478Lys
XM_006715411.1:c.25381C>A XP_006715474.1:p.Gln8461Lys
XM_006715412.1:c.25417C>A XP_006715475.1:p.Gln8473Lys
XM_006715413.1:c.25363C>A XP_006715476.1:p.Gln8455Lys
XM_006715414.1:c.25360C>A XP_006715477.1:p.Gln8454Lys
XM_006715415.1:c.25363C>A XP_006715478.1:p.Gln8455Lys
XM_006715416.1:c.25348C>A XP_006715479.1:p.Gln8450Lys
XM_006715417.1:c.25291C>A XP_006715480.1:p.Gln8431Lys
XM_006715420.1:c.25279C>A XP_006715483.1:p.Gln8427Lys
XM_006715421.1:c.25276C>A XP_006715484.1:p.Gln8426Lys
XM_006715422.1:c.25273C>A XP_006715485.1:p.Gln8425Lys
XM_006715423.1:c.25432C>A XP_006715486.1:p.Gln8478Lys
XM_006715424.1:c.25432C>A XP_006715487.1:p.Gln8478Lys
XM_006715425.1:c.25363C>A XP_006715488.1:p.Gln8455Lys
XM_011535641.1:c.25429C>A XP_011533943.1:p.Gln8477Lys
XM_011535642.1:c.25417C>A XP_011533944.1:p.Gln8473Lys
XM_011535643.1:c.25267C>A XP_011533945.1:p.Gln8423Lys
XM_011535644.1:c.23707C>A XP_011533946.1:p.Gln7903Lys
XM_011535645.1:c.23200C>A XP_011533947.1:p.Gln7734Lys
XM_011535647.1:c.18667C>A XP_011533949.1:p.Gln6223Lys
NM_001347701.1:c.1933C>A NP_001334630.1:p.Gln645Lys
NM_001347702.1:c.1861C>A NP_001334631.1:p.Gln621Lys
XM_006715408.2:c.25420C>A XP_006715471.1:p.Gln8474Lys
XM_006715410.2:c.25432C>A XP_006715473.1:p.Gln8478Lys
XM_006715412.2:c.25417C>A XP_006715475.1:p.Gln8473Lys
XM_006715413.2:c.25363C>A XP_006715476.1:p.Gln8455Lys
XM_006715415.2:c.25363C>A XP_006715478.1:p.Gln8455Lys
XM_006715416.2:c.25348C>A XP_006715479.1:p.Gln8450Lys
XM_006715417.2:c.25291C>A XP_006715480.1:p.Gln8431Lys
XM_006715420.2:c.25279C>A XP_006715483.1:p.Gln8427Lys
XM_006715421.2:c.25276C>A XP_006715484.1:p.Gln8426Lys
XM_006715423.2:c.25432C>A XP_006715486.1:p.Gln8478Lys
XM_006715424.2:c.25432C>A XP_006715487.1:p.Gln8478Lys
XM_006715425.2:c.25363C>A XP_006715488.1:p.Gln8455Lys
XM_011535641.2:c.25429C>A XP_011533943.1:p.Gln8477Lys
XM_011535642.2:c.25417C>A XP_011533944.1:p.Gln8473Lys
XM_011535645.2:c.23200C>A XP_011533947.1:p.Gln7734Lys
XM_017010608.1:c.25432C>A XP_016866097.1:p.Gln8478Lys
XM_017010609.1:c.25432C>A XP_016866098.1:p.Gln8478Lys
XM_017010610.1:c.25411C>A XP_016866099.1:p.Gln8471Lys
XM_017010611.2:c.25405C>A XP_016866100.1:p.Gln8469Lys
XM_017010612.1:c.25354C>A XP_016866101.1:p.Gln8452Lys
XM_017010613.1:c.25360C>A XP_016866102.1:p.Gln8454Lys
XM_017010614.1:c.25276C>A XP_016866103.1:p.Gln8426Lys
XM_017010615.1:c.25207C>A XP_016866104.1:p.Gln8403Lys
XM_017010616.1:c.25363C>A XP_016866105.1:p.Gln8455Lys
XM_017010617.1:c.25360C>A XP_016866106.1:p.Gln8454Lys
XM_017010618.1:c.25348C>A XP_016866107.1:p.Gln8450Lys
XM_017010619.1:c.23707C>A XP_016866108.1:p.Gln7903Lys
NM_182961.4:c.25327C>A MANE Select NP_892006.3:p.Gln8443Lys
NM_001347701.2:c.1933C>A NP_001334630.1:p.Gln645Lys
NM_001347702.2:c.1861C>A MANE Plus Clinical NP_001334631.1:p.Gln621Lys
NM_033071.5:c.25183C>A NP_149062.2:p.Gln8395Lys