Canonical Allele Identifier: CA366081236
Gene: SYNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152141209T>G , CM000668.2:g.152141209T>G GRCh38
NC_000006.11:g.152462344T>G , CM000668.1:g.152462344T>G GRCh37
NC_000006.10:g.152504037T>G NCBI36
NG_012855.1:g.501191A>C
NG_012855.2:g.501191A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354674.5:c.1774A>C MANE Plus Clinical ENSP00000346701.4:p.Thr592Pro
ENST00000367255.10:c.25240A>C MANE Select ENSP00000356224.5:p.Thr8414Pro
ENST00000423061.6:c.25096A>C ENSP00000396024.1:p.Thr8366Pro
ENST00000672154.1:c.642A>C
ENST00000672169.1:c.975A>C
ENST00000673173.1:c.891-1048A>C
ENST00000673451.1:c.1012A>C ENSP00000500189.1:p.Thr338Pro
ENST00000341594.9:c.24025A>C ENSP00000341887.6:p.Thr8009Pro
ENST00000347037.9:n.1988A>C
ENST00000354674.4:c.1774A>C ENSP00000346701.4:p.Thr592Pro
ENST00000367251.7:c.4075A>C ENSP00000356220.3:p.Thr1359Pro
ENST00000367255.9:c.25240A>C ENSP00000356224.5:p.Thr8414Pro
ENST00000367256.9:n.8932A>C
ENST00000367257.8:c.3178A>C ENSP00000356226.4:p.Thr1060Pro
ENST00000409694.6:n.8824A>C
ENST00000423061.5:c.25096A>C ENSP00000396024.1:p.Thr8366Pro
ENST00000460912.6:n.1854A>C
ENST00000478916.5:n.4262A>C
ENST00000536990.5:n.2077A>C
ENST00000539504.5:c.1705A>C ENSP00000441052.1:p.Thr569Pro
NM_033071.3:c.25096A>C NP_149062.1:p.Thr8366Pro
NM_182961.3:c.25240A>C NP_892006.3:p.Thr8414Pro
XM_006715407.1:c.25345A>C XP_006715470.1:p.Thr8449Pro
XM_006715408.1:c.25333A>C XP_006715471.1:p.Thr8445Pro
XM_006715409.1:c.25324A>C XP_006715472.1:p.Thr8442Pro
XM_006715410.1:c.25345A>C XP_006715473.1:p.Thr8449Pro
XM_006715411.1:c.25294A>C XP_006715474.1:p.Thr8432Pro
XM_006715412.1:c.25330A>C XP_006715475.1:p.Thr8444Pro
XM_006715413.1:c.25276A>C XP_006715476.1:p.Thr8426Pro
XM_006715414.1:c.25273A>C XP_006715477.1:p.Thr8425Pro
XM_006715415.1:c.25276A>C XP_006715478.1:p.Thr8426Pro
XM_006715416.1:c.25261A>C XP_006715479.1:p.Thr8421Pro
XM_006715417.1:c.25204A>C XP_006715480.1:p.Thr8402Pro
XM_006715420.1:c.25192A>C XP_006715483.1:p.Thr8398Pro
XM_006715421.1:c.25189A>C XP_006715484.1:p.Thr8397Pro
XM_006715422.1:c.25186A>C XP_006715485.1:p.Thr8396Pro
XM_006715423.1:c.25345A>C XP_006715486.1:p.Thr8449Pro
XM_006715424.1:c.25345A>C XP_006715487.1:p.Thr8449Pro
XM_006715425.1:c.25276A>C XP_006715488.1:p.Thr8426Pro
XM_011535641.1:c.25342A>C XP_011533943.1:p.Thr8448Pro
XM_011535642.1:c.25330A>C XP_011533944.1:p.Thr8444Pro
XM_011535643.1:c.25180A>C XP_011533945.1:p.Thr8394Pro
XM_011535644.1:c.23620A>C XP_011533946.1:p.Thr7874Pro
XM_011535645.1:c.23113A>C XP_011533947.1:p.Thr7705Pro
XM_011535647.1:c.18580A>C XP_011533949.1:p.Thr6194Pro
NM_001347701.1:c.1846A>C NP_001334630.1:p.Thr616Pro
NM_001347702.1:c.1774A>C NP_001334631.1:p.Thr592Pro
XM_006715408.2:c.25333A>C XP_006715471.1:p.Thr8445Pro
XM_006715410.2:c.25345A>C XP_006715473.1:p.Thr8449Pro
XM_006715412.2:c.25330A>C XP_006715475.1:p.Thr8444Pro
XM_006715413.2:c.25276A>C XP_006715476.1:p.Thr8426Pro
XM_006715415.2:c.25276A>C XP_006715478.1:p.Thr8426Pro
XM_006715416.2:c.25261A>C XP_006715479.1:p.Thr8421Pro
XM_006715417.2:c.25204A>C XP_006715480.1:p.Thr8402Pro
XM_006715420.2:c.25192A>C XP_006715483.1:p.Thr8398Pro
XM_006715421.2:c.25189A>C XP_006715484.1:p.Thr8397Pro
XM_006715423.2:c.25345A>C XP_006715486.1:p.Thr8449Pro
XM_006715424.2:c.25345A>C XP_006715487.1:p.Thr8449Pro
XM_006715425.2:c.25276A>C XP_006715488.1:p.Thr8426Pro
XM_011535641.2:c.25342A>C XP_011533943.1:p.Thr8448Pro
XM_011535642.2:c.25330A>C XP_011533944.1:p.Thr8444Pro
XM_011535645.2:c.23113A>C XP_011533947.1:p.Thr7705Pro
XM_017010608.1:c.25345A>C XP_016866097.1:p.Thr8449Pro
XM_017010609.1:c.25345A>C XP_016866098.1:p.Thr8449Pro
XM_017010610.1:c.25324A>C XP_016866099.1:p.Thr8442Pro
XM_017010611.2:c.25318A>C XP_016866100.1:p.Thr8440Pro
XM_017010612.1:c.25267A>C XP_016866101.1:p.Thr8423Pro
XM_017010613.1:c.25273A>C XP_016866102.1:p.Thr8425Pro
XM_017010614.1:c.25189A>C XP_016866103.1:p.Thr8397Pro
XM_017010615.1:c.25120A>C XP_016866104.1:p.Thr8374Pro
XM_017010616.1:c.25276A>C XP_016866105.1:p.Thr8426Pro
XM_017010617.1:c.25273A>C XP_016866106.1:p.Thr8425Pro
XM_017010618.1:c.25261A>C XP_016866107.1:p.Thr8421Pro
XM_017010619.1:c.23620A>C XP_016866108.1:p.Thr7874Pro
NM_182961.4:c.25240A>C MANE Select NP_892006.3:p.Thr8414Pro
NM_001347701.2:c.1846A>C NP_001334630.1:p.Thr616Pro
NM_001347702.2:c.1774A>C MANE Plus Clinical NP_001334631.1:p.Thr592Pro
NM_033071.5:c.25096A>C NP_149062.2:p.Thr8366Pro