Canonical Allele Identifier: CA1673206451
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152140153C= , CM000668.2:g.152140153C= GRCh38
NC_000006.11:g.152461288C= , CM000668.1:g.152461288C= GRCh37
NC_000006.10:g.152502981C= NCBI36
NG_012855.1:g.502247G=
NG_012855.2:g.502247G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1789G= MANE Plus Clinical ENSP00000346701.4:p.Asp597=
ENST00000367255.10:c.25255G= MANE Select ENSP00000356224.5:p.Asp8419=
ENST00000423061.6:c.25111G= ENSP00000396024.1:p.Asp8371=
ENST00000672154.1:c.657G=
ENST00000672169.1:c.990G=
ENST00000673173.1:c.899G=
ENST00000673451.1:c.1027G= ENSP00000500189.1:p.Asp343=
ENST00000341594.9:c.24040G= ENSP00000341887.6:p.Asp8014=
ENST00000347037.9:n.2003G=
ENST00000354674.4:c.1789G= ENSP00000346701.4:p.Asp597=
ENST00000367251.7:c.4090G= ENSP00000356220.3:p.Asp1364=
ENST00000367255.9:c.25255G= ENSP00000356224.5:p.Asp8419=
ENST00000367256.9:n.8947G=
ENST00000367257.8:c.3193G= ENSP00000356226.4:p.Asp1065=
ENST00000409694.6:n.8839G=
ENST00000423061.5:c.25111G= ENSP00000396024.1:p.Asp8371=
ENST00000460912.6:n.1869G=
ENST00000478916.5:n.4277G=
ENST00000536990.5:n.2092G=
ENST00000539504.5:c.1720G= ENSP00000441052.1:p.Asp574=
NM_033071.3:c.25111G= NP_149062.1:p.Asp8371=
NM_182961.3:c.25255G= NP_892006.3:p.Asp8419=
XM_006715407.1:c.25360G= XP_006715470.1:p.Asp8454=
XM_006715408.1:c.25348G= XP_006715471.1:p.Asp8450=
XM_006715409.1:c.25339G= XP_006715472.1:p.Asp8447=
XM_006715410.1:c.25360G= XP_006715473.1:p.Asp8454=
XM_006715411.1:c.25309G= XP_006715474.1:p.Asp8437=
XM_006715412.1:c.25345G= XP_006715475.1:p.Asp8449=
XM_006715413.1:c.25291G= XP_006715476.1:p.Asp8431=
XM_006715414.1:c.25288G= XP_006715477.1:p.Asp8430=
XM_006715415.1:c.25291G= XP_006715478.1:p.Asp8431=
XM_006715416.1:c.25276G= XP_006715479.1:p.Asp8426=
XM_006715417.1:c.25219G= XP_006715480.1:p.Asp8407=
XM_006715420.1:c.25207G= XP_006715483.1:p.Asp8403=
XM_006715421.1:c.25204G= XP_006715484.1:p.Asp8402=
XM_006715422.1:c.25201G= XP_006715485.1:p.Asp8401=
XM_006715423.1:c.25360G= XP_006715486.1:p.Asp8454=
XM_006715424.1:c.25360G= XP_006715487.1:p.Asp8454=
XM_006715425.1:c.25291G= XP_006715488.1:p.Asp8431=
XM_011535641.1:c.25357G= XP_011533943.1:p.Asp8453=
XM_011535642.1:c.25345G= XP_011533944.1:p.Asp8449=
XM_011535643.1:c.25195G= XP_011533945.1:p.Asp8399=
XM_011535644.1:c.23635G= XP_011533946.1:p.Asp7879=
XM_011535645.1:c.23128G= XP_011533947.1:p.Asp7710=
XM_011535647.1:c.18595G= XP_011533949.1:p.Asp6199=
NM_001347701.1:c.1861G= NP_001334630.1:p.Asp621=
NM_001347702.1:c.1789G= NP_001334631.1:p.Asp597=
XM_006715408.2:c.25348G= XP_006715471.1:p.Asp8450=
XM_006715410.2:c.25360G= XP_006715473.1:p.Asp8454=
XM_006715412.2:c.25345G= XP_006715475.1:p.Asp8449=
XM_006715413.2:c.25291G= XP_006715476.1:p.Asp8431=
XM_006715415.2:c.25291G= XP_006715478.1:p.Asp8431=
XM_006715416.2:c.25276G= XP_006715479.1:p.Asp8426=
XM_006715417.2:c.25219G= XP_006715480.1:p.Asp8407=
XM_006715420.2:c.25207G= XP_006715483.1:p.Asp8403=
XM_006715421.2:c.25204G= XP_006715484.1:p.Asp8402=
XM_006715423.2:c.25360G= XP_006715486.1:p.Asp8454=
XM_006715424.2:c.25360G= XP_006715487.1:p.Asp8454=
XM_006715425.2:c.25291G= XP_006715488.1:p.Asp8431=
XM_011535641.2:c.25357G= XP_011533943.1:p.Asp8453=
XM_011535642.2:c.25345G= XP_011533944.1:p.Asp8449=
XM_011535645.2:c.23128G= XP_011533947.1:p.Asp7710=
XM_017010608.1:c.25360G= XP_016866097.1:p.Asp8454=
XM_017010609.1:c.25360G= XP_016866098.1:p.Asp8454=
XM_017010610.1:c.25339G= XP_016866099.1:p.Asp8447=
XM_017010611.2:c.25333G= XP_016866100.1:p.Asp8445=
XM_017010612.1:c.25282G= XP_016866101.1:p.Asp8428=
XM_017010613.1:c.25288G= XP_016866102.1:p.Asp8430=
XM_017010614.1:c.25204G= XP_016866103.1:p.Asp8402=
XM_017010615.1:c.25135G= XP_016866104.1:p.Asp8379=
XM_017010616.1:c.25291G= XP_016866105.1:p.Asp8431=
XM_017010617.1:c.25288G= XP_016866106.1:p.Asp8430=
XM_017010618.1:c.25276G= XP_016866107.1:p.Asp8426=
XM_017010619.1:c.23635G= XP_016866108.1:p.Asp7879=
NM_182961.4:c.25255G= MANE Select NP_892006.3:p.Asp8419=
NM_001347701.2:c.1861G= NP_001334630.1:p.Asp621=
NM_001347702.2:c.1789G= MANE Plus Clinical NP_001334631.1:p.Asp597=
NM_033071.5:c.25111G= NP_149062.2:p.Asp8371=