Canonical Allele Identifier: CA366080038
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152139982G>T , CM000668.2:g.152139982G>T GRCh38
NC_000006.11:g.152461117G>T , CM000668.1:g.152461117G>T GRCh37
NC_000006.10:g.152502810G>T NCBI36
NG_012855.1:g.502418C>A
NG_012855.2:g.502418C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1960C>A MANE Plus Clinical ENSP00000346701.4:p.Gln654Lys
ENST00000367255.10:c.25426C>A MANE Select ENSP00000356224.5:p.Gln8476Lys
ENST00000423061.6:c.25282C>A ENSP00000396024.1:p.Gln8428Lys
ENST00000672154.1:c.828C>A
ENST00000672169.1:c.1161C>A
ENST00000673173.1:c.1070C>A
ENST00000673451.1:c.1198C>A ENSP00000500189.1:p.Gln400Lys
ENST00000341594.9:c.24211C>A ENSP00000341887.6:p.Gln8071Lys
ENST00000347037.9:n.2174C>A
ENST00000354674.4:c.1960C>A ENSP00000346701.4:p.Gln654Lys
ENST00000367251.7:c.4261C>A ENSP00000356220.3:p.Gln1421Lys
ENST00000367255.9:c.25426C>A ENSP00000356224.5:p.Gln8476Lys
ENST00000367256.9:n.9118C>A
ENST00000367257.8:c.3364C>A ENSP00000356226.4:p.Gln1122Lys
ENST00000409694.6:n.9010C>A
ENST00000423061.5:c.25282C>A ENSP00000396024.1:p.Gln8428Lys
ENST00000460912.6:n.2040C>A
ENST00000478916.5:n.4448C>A
ENST00000536990.5:n.2263C>A
ENST00000539504.5:c.1891C>A ENSP00000441052.1:p.Gln631Lys
NM_033071.3:c.25282C>A NP_149062.1:p.Gln8428Lys
NM_182961.3:c.25426C>A NP_892006.3:p.Gln8476Lys
XM_006715407.1:c.25531C>A XP_006715470.1:p.Gln8511Lys
XM_006715408.1:c.25519C>A XP_006715471.1:p.Gln8507Lys
XM_006715409.1:c.25510C>A XP_006715472.1:p.Gln8504Lys
XM_006715410.1:c.25531C>A XP_006715473.1:p.Gln8511Lys
XM_006715411.1:c.25480C>A XP_006715474.1:p.Gln8494Lys
XM_006715412.1:c.25516C>A XP_006715475.1:p.Gln8506Lys
XM_006715413.1:c.25462C>A XP_006715476.1:p.Gln8488Lys
XM_006715414.1:c.25459C>A XP_006715477.1:p.Gln8487Lys
XM_006715415.1:c.25462C>A XP_006715478.1:p.Gln8488Lys
XM_006715416.1:c.25447C>A XP_006715479.1:p.Gln8483Lys
XM_006715417.1:c.25390C>A XP_006715480.1:p.Gln8464Lys
XM_006715420.1:c.25378C>A XP_006715483.1:p.Gln8460Lys
XM_006715421.1:c.25375C>A XP_006715484.1:p.Gln8459Lys
XM_006715422.1:c.25372C>A XP_006715485.1:p.Gln8458Lys
XM_006715423.1:c.25531C>A XP_006715486.1:p.Gln8511Lys
XM_006715424.1:c.25531C>A XP_006715487.1:p.Gln8511Lys
XM_006715425.1:c.25462C>A XP_006715488.1:p.Gln8488Lys
XM_011535641.1:c.25528C>A XP_011533943.1:p.Gln8510Lys
XM_011535642.1:c.25516C>A XP_011533944.1:p.Gln8506Lys
XM_011535643.1:c.25366C>A XP_011533945.1:p.Gln8456Lys
XM_011535644.1:c.23806C>A XP_011533946.1:p.Gln7936Lys
XM_011535645.1:c.23299C>A XP_011533947.1:p.Gln7767Lys
XM_011535647.1:c.18766C>A XP_011533949.1:p.Gln6256Lys
NM_001347701.1:c.2032C>A NP_001334630.1:p.Gln678Lys
NM_001347702.1:c.1960C>A NP_001334631.1:p.Gln654Lys
XM_006715408.2:c.25519C>A XP_006715471.1:p.Gln8507Lys
XM_006715410.2:c.25531C>A XP_006715473.1:p.Gln8511Lys
XM_006715412.2:c.25516C>A XP_006715475.1:p.Gln8506Lys
XM_006715413.2:c.25462C>A XP_006715476.1:p.Gln8488Lys
XM_006715415.2:c.25462C>A XP_006715478.1:p.Gln8488Lys
XM_006715416.2:c.25447C>A XP_006715479.1:p.Gln8483Lys
XM_006715417.2:c.25390C>A XP_006715480.1:p.Gln8464Lys
XM_006715420.2:c.25378C>A XP_006715483.1:p.Gln8460Lys
XM_006715421.2:c.25375C>A XP_006715484.1:p.Gln8459Lys
XM_006715423.2:c.25531C>A XP_006715486.1:p.Gln8511Lys
XM_006715424.2:c.25531C>A XP_006715487.1:p.Gln8511Lys
XM_006715425.2:c.25462C>A XP_006715488.1:p.Gln8488Lys
XM_011535641.2:c.25528C>A XP_011533943.1:p.Gln8510Lys
XM_011535642.2:c.25516C>A XP_011533944.1:p.Gln8506Lys
XM_011535645.2:c.23299C>A XP_011533947.1:p.Gln7767Lys
XM_017010608.1:c.25531C>A XP_016866097.1:p.Gln8511Lys
XM_017010609.1:c.25531C>A XP_016866098.1:p.Gln8511Lys
XM_017010610.1:c.25510C>A XP_016866099.1:p.Gln8504Lys
XM_017010611.2:c.25504C>A XP_016866100.1:p.Gln8502Lys
XM_017010612.1:c.25453C>A XP_016866101.1:p.Gln8485Lys
XM_017010613.1:c.25459C>A XP_016866102.1:p.Gln8487Lys
XM_017010614.1:c.25375C>A XP_016866103.1:p.Gln8459Lys
XM_017010615.1:c.25306C>A XP_016866104.1:p.Gln8436Lys
XM_017010616.1:c.25462C>A XP_016866105.1:p.Gln8488Lys
XM_017010617.1:c.25459C>A XP_016866106.1:p.Gln8487Lys
XM_017010618.1:c.25447C>A XP_016866107.1:p.Gln8483Lys
XM_017010619.1:c.23806C>A XP_016866108.1:p.Gln7936Lys
NM_182961.4:c.25426C>A MANE Select NP_892006.3:p.Gln8476Lys
NM_001347701.2:c.2032C>A NP_001334630.1:p.Gln678Lys
NM_001347702.2:c.1960C>A MANE Plus Clinical NP_001334631.1:p.Gln654Lys
NM_033071.5:c.25282C>A NP_149062.2:p.Gln8428Lys