Canonical Allele Identifier: CA366080107
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152139999T>G , CM000668.2:g.152139999T>G GRCh38
NC_000006.11:g.152461134T>G , CM000668.1:g.152461134T>G GRCh37
NC_000006.10:g.152502827T>G NCBI36
NG_012855.1:g.502401A>C
NG_012855.2:g.502401A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1943A>C MANE Plus Clinical ENSP00000346701.4:p.Glu648Ala
ENST00000367255.10:c.25409A>C MANE Select ENSP00000356224.5:p.Glu8470Ala
ENST00000423061.6:c.25265A>C ENSP00000396024.1:p.Glu8422Ala
ENST00000672154.1:c.811A>C
ENST00000672169.1:c.1144A>C
ENST00000673173.1:c.1053A>C
ENST00000673451.1:c.1181A>C ENSP00000500189.1:p.Glu394Ala
ENST00000341594.9:c.24194A>C ENSP00000341887.6:p.Glu8065Ala
ENST00000347037.9:n.2157A>C
ENST00000354674.4:c.1943A>C ENSP00000346701.4:p.Glu648Ala
ENST00000367251.7:c.4244A>C ENSP00000356220.3:p.Glu1415Ala
ENST00000367255.9:c.25409A>C ENSP00000356224.5:p.Glu8470Ala
ENST00000367256.9:n.9101A>C
ENST00000367257.8:c.3347A>C ENSP00000356226.4:p.Glu1116Ala
ENST00000409694.6:n.8993A>C
ENST00000423061.5:c.25265A>C ENSP00000396024.1:p.Glu8422Ala
ENST00000460912.6:n.2023A>C
ENST00000478916.5:n.4431A>C
ENST00000536990.5:n.2246A>C
ENST00000539504.5:c.1874A>C ENSP00000441052.1:p.Glu625Ala
NM_033071.3:c.25265A>C NP_149062.1:p.Glu8422Ala
NM_182961.3:c.25409A>C NP_892006.3:p.Glu8470Ala
XM_006715407.1:c.25514A>C XP_006715470.1:p.Glu8505Ala
XM_006715408.1:c.25502A>C XP_006715471.1:p.Glu8501Ala
XM_006715409.1:c.25493A>C XP_006715472.1:p.Glu8498Ala
XM_006715410.1:c.25514A>C XP_006715473.1:p.Glu8505Ala
XM_006715411.1:c.25463A>C XP_006715474.1:p.Glu8488Ala
XM_006715412.1:c.25499A>C XP_006715475.1:p.Glu8500Ala
XM_006715413.1:c.25445A>C XP_006715476.1:p.Glu8482Ala
XM_006715414.1:c.25442A>C XP_006715477.1:p.Glu8481Ala
XM_006715415.1:c.25445A>C XP_006715478.1:p.Glu8482Ala
XM_006715416.1:c.25430A>C XP_006715479.1:p.Glu8477Ala
XM_006715417.1:c.25373A>C XP_006715480.1:p.Glu8458Ala
XM_006715420.1:c.25361A>C XP_006715483.1:p.Glu8454Ala
XM_006715421.1:c.25358A>C XP_006715484.1:p.Glu8453Ala
XM_006715422.1:c.25355A>C XP_006715485.1:p.Glu8452Ala
XM_006715423.1:c.25514A>C XP_006715486.1:p.Glu8505Ala
XM_006715424.1:c.25514A>C XP_006715487.1:p.Glu8505Ala
XM_006715425.1:c.25445A>C XP_006715488.1:p.Glu8482Ala
XM_011535641.1:c.25511A>C XP_011533943.1:p.Glu8504Ala
XM_011535642.1:c.25499A>C XP_011533944.1:p.Glu8500Ala
XM_011535643.1:c.25349A>C XP_011533945.1:p.Glu8450Ala
XM_011535644.1:c.23789A>C XP_011533946.1:p.Glu7930Ala
XM_011535645.1:c.23282A>C XP_011533947.1:p.Glu7761Ala
XM_011535647.1:c.18749A>C XP_011533949.1:p.Glu6250Ala
NM_001347701.1:c.2015A>C NP_001334630.1:p.Glu672Ala
NM_001347702.1:c.1943A>C NP_001334631.1:p.Glu648Ala
XM_006715408.2:c.25502A>C XP_006715471.1:p.Glu8501Ala
XM_006715410.2:c.25514A>C XP_006715473.1:p.Glu8505Ala
XM_006715412.2:c.25499A>C XP_006715475.1:p.Glu8500Ala
XM_006715413.2:c.25445A>C XP_006715476.1:p.Glu8482Ala
XM_006715415.2:c.25445A>C XP_006715478.1:p.Glu8482Ala
XM_006715416.2:c.25430A>C XP_006715479.1:p.Glu8477Ala
XM_006715417.2:c.25373A>C XP_006715480.1:p.Glu8458Ala
XM_006715420.2:c.25361A>C XP_006715483.1:p.Glu8454Ala
XM_006715421.2:c.25358A>C XP_006715484.1:p.Glu8453Ala
XM_006715423.2:c.25514A>C XP_006715486.1:p.Glu8505Ala
XM_006715424.2:c.25514A>C XP_006715487.1:p.Glu8505Ala
XM_006715425.2:c.25445A>C XP_006715488.1:p.Glu8482Ala
XM_011535641.2:c.25511A>C XP_011533943.1:p.Glu8504Ala
XM_011535642.2:c.25499A>C XP_011533944.1:p.Glu8500Ala
XM_011535645.2:c.23282A>C XP_011533947.1:p.Glu7761Ala
XM_017010608.1:c.25514A>C XP_016866097.1:p.Glu8505Ala
XM_017010609.1:c.25514A>C XP_016866098.1:p.Glu8505Ala
XM_017010610.1:c.25493A>C XP_016866099.1:p.Glu8498Ala
XM_017010611.2:c.25487A>C XP_016866100.1:p.Glu8496Ala
XM_017010612.1:c.25436A>C XP_016866101.1:p.Glu8479Ala
XM_017010613.1:c.25442A>C XP_016866102.1:p.Glu8481Ala
XM_017010614.1:c.25358A>C XP_016866103.1:p.Glu8453Ala
XM_017010615.1:c.25289A>C XP_016866104.1:p.Glu8430Ala
XM_017010616.1:c.25445A>C XP_016866105.1:p.Glu8482Ala
XM_017010617.1:c.25442A>C XP_016866106.1:p.Glu8481Ala
XM_017010618.1:c.25430A>C XP_016866107.1:p.Glu8477Ala
XM_017010619.1:c.23789A>C XP_016866108.1:p.Glu7930Ala
NM_182961.4:c.25409A>C MANE Select NP_892006.3:p.Glu8470Ala
NM_001347701.2:c.2015A>C NP_001334630.1:p.Glu672Ala
NM_001347702.2:c.1943A>C MANE Plus Clinical NP_001334631.1:p.Glu648Ala
NM_033071.5:c.25265A>C NP_149062.2:p.Glu8422Ala