Canonical Allele Identifier: CA1673207679
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152141266T= , CM000668.2:g.152141266T= GRCh38
NC_000006.11:g.152462401T= , CM000668.1:g.152462401T= GRCh37
NC_000006.10:g.152504094T= NCBI36
NG_012855.1:g.501134A=
NG_012855.2:g.501134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354674.5:c.1717A= MANE Plus Clinical ENSP00000346701.4:p.Lys573=
ENST00000367255.10:c.25183A= MANE Select ENSP00000356224.5:p.Lys8395=
ENST00000423061.6:c.25039A= ENSP00000396024.1:p.Lys8347=
ENST00000672154.1:c.585A=
ENST00000672169.1:c.918A=
ENST00000673173.1:c.891-1105A=
ENST00000673451.1:c.955A= ENSP00000500189.1:p.Lys319=
ENST00000341594.9:c.23968A= ENSP00000341887.6:p.Lys7990=
ENST00000347037.9:n.1931A=
ENST00000354674.4:c.1717A= ENSP00000346701.4:p.Lys573=
ENST00000367251.7:c.4018A= ENSP00000356220.3:p.Lys1340=
ENST00000367255.9:c.25183A= ENSP00000356224.5:p.Lys8395=
ENST00000367256.9:n.8875A=
ENST00000367257.8:c.3121A= ENSP00000356226.4:p.Lys1041=
ENST00000409694.6:n.8767A=
ENST00000423061.5:c.25039A= ENSP00000396024.1:p.Lys8347=
ENST00000460912.6:n.1797A=
ENST00000478916.5:n.4205A=
ENST00000536990.5:n.2020A=
ENST00000539504.5:c.1648A= ENSP00000441052.1:p.Lys550=
NM_033071.3:c.25039A= NP_149062.1:p.Lys8347=
NM_182961.3:c.25183A= NP_892006.3:p.Lys8395=
XM_006715407.1:c.25288A= XP_006715470.1:p.Lys8430=
XM_006715408.1:c.25276A= XP_006715471.1:p.Lys8426=
XM_006715409.1:c.25267A= XP_006715472.1:p.Lys8423=
XM_006715410.1:c.25288A= XP_006715473.1:p.Lys8430=
XM_006715411.1:c.25237A= XP_006715474.1:p.Lys8413=
XM_006715412.1:c.25273A= XP_006715475.1:p.Lys8425=
XM_006715413.1:c.25219A= XP_006715476.1:p.Lys8407=
XM_006715414.1:c.25216A= XP_006715477.1:p.Lys8406=
XM_006715415.1:c.25219A= XP_006715478.1:p.Lys8407=
XM_006715416.1:c.25204A= XP_006715479.1:p.Lys8402=
XM_006715417.1:c.25147A= XP_006715480.1:p.Lys8383=
XM_006715420.1:c.25135A= XP_006715483.1:p.Lys8379=
XM_006715421.1:c.25132A= XP_006715484.1:p.Lys8378=
XM_006715422.1:c.25129A= XP_006715485.1:p.Lys8377=
XM_006715423.1:c.25288A= XP_006715486.1:p.Lys8430=
XM_006715424.1:c.25288A= XP_006715487.1:p.Lys8430=
XM_006715425.1:c.25219A= XP_006715488.1:p.Lys8407=
XM_011535641.1:c.25285A= XP_011533943.1:p.Lys8429=
XM_011535642.1:c.25273A= XP_011533944.1:p.Lys8425=
XM_011535643.1:c.25123A= XP_011533945.1:p.Lys8375=
XM_011535644.1:c.23563A= XP_011533946.1:p.Lys7855=
XM_011535645.1:c.23056A= XP_011533947.1:p.Lys7686=
XM_011535647.1:c.18523A= XP_011533949.1:p.Lys6175=
NM_001347701.1:c.1789A= NP_001334630.1:p.Lys597=
NM_001347702.1:c.1717A= NP_001334631.1:p.Lys573=
XM_006715408.2:c.25276A= XP_006715471.1:p.Lys8426=
XM_006715410.2:c.25288A= XP_006715473.1:p.Lys8430=
XM_006715412.2:c.25273A= XP_006715475.1:p.Lys8425=
XM_006715413.2:c.25219A= XP_006715476.1:p.Lys8407=
XM_006715415.2:c.25219A= XP_006715478.1:p.Lys8407=
XM_006715416.2:c.25204A= XP_006715479.1:p.Lys8402=
XM_006715417.2:c.25147A= XP_006715480.1:p.Lys8383=
XM_006715420.2:c.25135A= XP_006715483.1:p.Lys8379=
XM_006715421.2:c.25132A= XP_006715484.1:p.Lys8378=
XM_006715423.2:c.25288A= XP_006715486.1:p.Lys8430=
XM_006715424.2:c.25288A= XP_006715487.1:p.Lys8430=
XM_006715425.2:c.25219A= XP_006715488.1:p.Lys8407=
XM_011535641.2:c.25285A= XP_011533943.1:p.Lys8429=
XM_011535642.2:c.25273A= XP_011533944.1:p.Lys8425=
XM_011535645.2:c.23056A= XP_011533947.1:p.Lys7686=
XM_017010608.1:c.25288A= XP_016866097.1:p.Lys8430=
XM_017010609.1:c.25288A= XP_016866098.1:p.Lys8430=
XM_017010610.1:c.25267A= XP_016866099.1:p.Lys8423=
XM_017010611.2:c.25261A= XP_016866100.1:p.Lys8421=
XM_017010612.1:c.25210A= XP_016866101.1:p.Lys8404=
XM_017010613.1:c.25216A= XP_016866102.1:p.Lys8406=
XM_017010614.1:c.25132A= XP_016866103.1:p.Lys8378=
XM_017010615.1:c.25063A= XP_016866104.1:p.Lys8355=
XM_017010616.1:c.25219A= XP_016866105.1:p.Lys8407=
XM_017010617.1:c.25216A= XP_016866106.1:p.Lys8406=
XM_017010618.1:c.25204A= XP_016866107.1:p.Lys8402=
XM_017010619.1:c.23563A= XP_016866108.1:p.Lys7855=
NM_182961.4:c.25183A= MANE Select NP_892006.3:p.Lys8395=
NM_001347701.2:c.1789A= NP_001334630.1:p.Lys597=
NM_001347702.2:c.1717A= MANE Plus Clinical NP_001334631.1:p.Lys573=
NM_033071.5:c.25039A= NP_149062.2:p.Lys8347=