Canonical Allele Identifier: CA1673207781
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152141311A= , CM000668.2:g.152141311A= GRCh38
NC_000006.11:g.152462446A= , CM000668.1:g.152462446A= GRCh37
NC_000006.10:g.152504139A= NCBI36
NG_012855.1:g.501089T=
NG_012855.2:g.501089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1672T= MANE Plus Clinical ENSP00000346701.4:p.Cys558=
ENST00000367255.10:c.25138T= MANE Select ENSP00000356224.5:p.Cys8380=
ENST00000423061.6:c.24994T= ENSP00000396024.1:p.Cys8332=
ENST00000672154.1:c.540T=
ENST00000672169.1:c.873T=
ENST00000673173.1:c.891-1150T=
ENST00000673451.1:c.910T= ENSP00000500189.1:p.Cys304=
ENST00000341594.9:c.23923T= ENSP00000341887.6:p.Cys7975=
ENST00000347037.9:n.1886T=
ENST00000354674.4:c.1672T= ENSP00000346701.4:p.Cys558=
ENST00000367251.7:c.3973T= ENSP00000356220.3:p.Cys1325=
ENST00000367255.9:c.25138T= ENSP00000356224.5:p.Cys8380=
ENST00000367256.9:n.8830T=
ENST00000367257.8:c.3076T= ENSP00000356226.4:p.Cys1026=
ENST00000409694.6:n.8722T=
ENST00000423061.5:c.24994T= ENSP00000396024.1:p.Cys8332=
ENST00000460912.6:n.1752T=
ENST00000478916.5:n.4160T=
ENST00000536990.5:n.1975T=
ENST00000539504.5:c.1603T= ENSP00000441052.1:p.Cys535=
NM_033071.3:c.24994T= NP_149062.1:p.Cys8332=
NM_182961.3:c.25138T= NP_892006.3:p.Cys8380=
XM_006715407.1:c.25243T= XP_006715470.1:p.Cys8415=
XM_006715408.1:c.25231T= XP_006715471.1:p.Cys8411=
XM_006715409.1:c.25222T= XP_006715472.1:p.Cys8408=
XM_006715410.1:c.25243T= XP_006715473.1:p.Cys8415=
XM_006715411.1:c.25192T= XP_006715474.1:p.Cys8398=
XM_006715412.1:c.25228T= XP_006715475.1:p.Cys8410=
XM_006715413.1:c.25174T= XP_006715476.1:p.Cys8392=
XM_006715414.1:c.25171T= XP_006715477.1:p.Cys8391=
XM_006715415.1:c.25174T= XP_006715478.1:p.Cys8392=
XM_006715416.1:c.25159T= XP_006715479.1:p.Cys8387=
XM_006715417.1:c.25102T= XP_006715480.1:p.Cys8368=
XM_006715420.1:c.25090T= XP_006715483.1:p.Cys8364=
XM_006715421.1:c.25087T= XP_006715484.1:p.Cys8363=
XM_006715422.1:c.25084T= XP_006715485.1:p.Cys8362=
XM_006715423.1:c.25243T= XP_006715486.1:p.Cys8415=
XM_006715424.1:c.25243T= XP_006715487.1:p.Cys8415=
XM_006715425.1:c.25174T= XP_006715488.1:p.Cys8392=
XM_011535641.1:c.25240T= XP_011533943.1:p.Cys8414=
XM_011535642.1:c.25228T= XP_011533944.1:p.Cys8410=
XM_011535643.1:c.25078T= XP_011533945.1:p.Cys8360=
XM_011535644.1:c.23518T= XP_011533946.1:p.Cys7840=
XM_011535645.1:c.23011T= XP_011533947.1:p.Cys7671=
XM_011535647.1:c.18478T= XP_011533949.1:p.Cys6160=
NM_001347701.1:c.1744T= NP_001334630.1:p.Cys582=
NM_001347702.1:c.1672T= NP_001334631.1:p.Cys558=
XM_006715408.2:c.25231T= XP_006715471.1:p.Cys8411=
XM_006715410.2:c.25243T= XP_006715473.1:p.Cys8415=
XM_006715412.2:c.25228T= XP_006715475.1:p.Cys8410=
XM_006715413.2:c.25174T= XP_006715476.1:p.Cys8392=
XM_006715415.2:c.25174T= XP_006715478.1:p.Cys8392=
XM_006715416.2:c.25159T= XP_006715479.1:p.Cys8387=
XM_006715417.2:c.25102T= XP_006715480.1:p.Cys8368=
XM_006715420.2:c.25090T= XP_006715483.1:p.Cys8364=
XM_006715421.2:c.25087T= XP_006715484.1:p.Cys8363=
XM_006715423.2:c.25243T= XP_006715486.1:p.Cys8415=
XM_006715424.2:c.25243T= XP_006715487.1:p.Cys8415=
XM_006715425.2:c.25174T= XP_006715488.1:p.Cys8392=
XM_011535641.2:c.25240T= XP_011533943.1:p.Cys8414=
XM_011535642.2:c.25228T= XP_011533944.1:p.Cys8410=
XM_011535645.2:c.23011T= XP_011533947.1:p.Cys7671=
XM_017010608.1:c.25243T= XP_016866097.1:p.Cys8415=
XM_017010609.1:c.25243T= XP_016866098.1:p.Cys8415=
XM_017010610.1:c.25222T= XP_016866099.1:p.Cys8408=
XM_017010611.2:c.25216T= XP_016866100.1:p.Cys8406=
XM_017010612.1:c.25165T= XP_016866101.1:p.Cys8389=
XM_017010613.1:c.25171T= XP_016866102.1:p.Cys8391=
XM_017010614.1:c.25087T= XP_016866103.1:p.Cys8363=
XM_017010615.1:c.25018T= XP_016866104.1:p.Cys8340=
XM_017010616.1:c.25174T= XP_016866105.1:p.Cys8392=
XM_017010617.1:c.25171T= XP_016866106.1:p.Cys8391=
XM_017010618.1:c.25159T= XP_016866107.1:p.Cys8387=
XM_017010619.1:c.23518T= XP_016866108.1:p.Cys7840=
NM_182961.4:c.25138T= MANE Select NP_892006.3:p.Cys8380=
NM_001347701.2:c.1744T= NP_001334630.1:p.Cys582=
NM_001347702.2:c.1672T= MANE Plus Clinical NP_001334631.1:p.Cys558=
NM_033071.5:c.24994T= NP_149062.2:p.Cys8332=