Canonical Allele Identifier: CA366080520
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152140078G>T , CM000668.2:g.152140078G>T GRCh38
NC_000006.11:g.152461213G>T , CM000668.1:g.152461213G>T GRCh37
NC_000006.10:g.152502906G>T NCBI36
NG_012855.1:g.502322C>A
NG_012855.2:g.502322C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1864C>A MANE Plus Clinical ENSP00000346701.4:p.Gln622Lys
ENST00000367255.10:c.25330C>A MANE Select ENSP00000356224.5:p.Gln8444Lys
ENST00000423061.6:c.25186C>A ENSP00000396024.1:p.Gln8396Lys
ENST00000672154.1:c.732C>A
ENST00000672169.1:c.1065C>A
ENST00000673173.1:c.974C>A
ENST00000673451.1:c.1102C>A ENSP00000500189.1:p.Gln368Lys
ENST00000341594.9:c.24115C>A ENSP00000341887.6:p.Gln8039Lys
ENST00000347037.9:n.2078C>A
ENST00000354674.4:c.1864C>A ENSP00000346701.4:p.Gln622Lys
ENST00000367251.7:c.4165C>A ENSP00000356220.3:p.Gln1389Lys
ENST00000367255.9:c.25330C>A ENSP00000356224.5:p.Gln8444Lys
ENST00000367256.9:n.9022C>A
ENST00000367257.8:c.3268C>A ENSP00000356226.4:p.Gln1090Lys
ENST00000409694.6:n.8914C>A
ENST00000423061.5:c.25186C>A ENSP00000396024.1:p.Gln8396Lys
ENST00000460912.6:n.1944C>A
ENST00000478916.5:n.4352C>A
ENST00000536990.5:n.2167C>A
ENST00000539504.5:c.1795C>A ENSP00000441052.1:p.Gln599Lys
NM_033071.3:c.25186C>A NP_149062.1:p.Gln8396Lys
NM_182961.3:c.25330C>A NP_892006.3:p.Gln8444Lys
XM_006715407.1:c.25435C>A XP_006715470.1:p.Gln8479Lys
XM_006715408.1:c.25423C>A XP_006715471.1:p.Gln8475Lys
XM_006715409.1:c.25414C>A XP_006715472.1:p.Gln8472Lys
XM_006715410.1:c.25435C>A XP_006715473.1:p.Gln8479Lys
XM_006715411.1:c.25384C>A XP_006715474.1:p.Gln8462Lys
XM_006715412.1:c.25420C>A XP_006715475.1:p.Gln8474Lys
XM_006715413.1:c.25366C>A XP_006715476.1:p.Gln8456Lys
XM_006715414.1:c.25363C>A XP_006715477.1:p.Gln8455Lys
XM_006715415.1:c.25366C>A XP_006715478.1:p.Gln8456Lys
XM_006715416.1:c.25351C>A XP_006715479.1:p.Gln8451Lys
XM_006715417.1:c.25294C>A XP_006715480.1:p.Gln8432Lys
XM_006715420.1:c.25282C>A XP_006715483.1:p.Gln8428Lys
XM_006715421.1:c.25279C>A XP_006715484.1:p.Gln8427Lys
XM_006715422.1:c.25276C>A XP_006715485.1:p.Gln8426Lys
XM_006715423.1:c.25435C>A XP_006715486.1:p.Gln8479Lys
XM_006715424.1:c.25435C>A XP_006715487.1:p.Gln8479Lys
XM_006715425.1:c.25366C>A XP_006715488.1:p.Gln8456Lys
XM_011535641.1:c.25432C>A XP_011533943.1:p.Gln8478Lys
XM_011535642.1:c.25420C>A XP_011533944.1:p.Gln8474Lys
XM_011535643.1:c.25270C>A XP_011533945.1:p.Gln8424Lys
XM_011535644.1:c.23710C>A XP_011533946.1:p.Gln7904Lys
XM_011535645.1:c.23203C>A XP_011533947.1:p.Gln7735Lys
XM_011535647.1:c.18670C>A XP_011533949.1:p.Gln6224Lys
NM_001347701.1:c.1936C>A NP_001334630.1:p.Gln646Lys
NM_001347702.1:c.1864C>A NP_001334631.1:p.Gln622Lys
XM_006715408.2:c.25423C>A XP_006715471.1:p.Gln8475Lys
XM_006715410.2:c.25435C>A XP_006715473.1:p.Gln8479Lys
XM_006715412.2:c.25420C>A XP_006715475.1:p.Gln8474Lys
XM_006715413.2:c.25366C>A XP_006715476.1:p.Gln8456Lys
XM_006715415.2:c.25366C>A XP_006715478.1:p.Gln8456Lys
XM_006715416.2:c.25351C>A XP_006715479.1:p.Gln8451Lys
XM_006715417.2:c.25294C>A XP_006715480.1:p.Gln8432Lys
XM_006715420.2:c.25282C>A XP_006715483.1:p.Gln8428Lys
XM_006715421.2:c.25279C>A XP_006715484.1:p.Gln8427Lys
XM_006715423.2:c.25435C>A XP_006715486.1:p.Gln8479Lys
XM_006715424.2:c.25435C>A XP_006715487.1:p.Gln8479Lys
XM_006715425.2:c.25366C>A XP_006715488.1:p.Gln8456Lys
XM_011535641.2:c.25432C>A XP_011533943.1:p.Gln8478Lys
XM_011535642.2:c.25420C>A XP_011533944.1:p.Gln8474Lys
XM_011535645.2:c.23203C>A XP_011533947.1:p.Gln7735Lys
XM_017010608.1:c.25435C>A XP_016866097.1:p.Gln8479Lys
XM_017010609.1:c.25435C>A XP_016866098.1:p.Gln8479Lys
XM_017010610.1:c.25414C>A XP_016866099.1:p.Gln8472Lys
XM_017010611.2:c.25408C>A XP_016866100.1:p.Gln8470Lys
XM_017010612.1:c.25357C>A XP_016866101.1:p.Gln8453Lys
XM_017010613.1:c.25363C>A XP_016866102.1:p.Gln8455Lys
XM_017010614.1:c.25279C>A XP_016866103.1:p.Gln8427Lys
XM_017010615.1:c.25210C>A XP_016866104.1:p.Gln8404Lys
XM_017010616.1:c.25366C>A XP_016866105.1:p.Gln8456Lys
XM_017010617.1:c.25363C>A XP_016866106.1:p.Gln8455Lys
XM_017010618.1:c.25351C>A XP_016866107.1:p.Gln8451Lys
XM_017010619.1:c.23710C>A XP_016866108.1:p.Gln7904Lys
NM_182961.4:c.25330C>A MANE Select NP_892006.3:p.Gln8444Lys
NM_001347701.2:c.1936C>A NP_001334630.1:p.Gln646Lys
NM_001347702.2:c.1864C>A MANE Plus Clinical NP_001334631.1:p.Gln622Lys
NM_033071.5:c.25186C>A NP_149062.2:p.Gln8396Lys