Canonical Allele Identifier: CA366081018

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461286G>C (hg19) ; chr6:g.152140151G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140151G>C , CM000668.2:g.152140151G>C	GRCh38
NC_000006.11:g.152461286G>C , CM000668.1:g.152461286G>C	GRCh37
NC_000006.10:g.152502979G>C	NCBI36
NG_012855.1:g.502249C>G
NG_012855.2:g.502249C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1791C>G MANE Plus Clinical	ENSP00000346701.4:p.Asp597Glu
ENST00000367255.10:c.25257C>G MANE Select	ENSP00000356224.5:p.Asp8419Glu
ENST00000423061.6:c.25113C>G	ENSP00000396024.1:p.Asp8371Glu
ENST00000672154.1:c.659C>G
ENST00000672169.1:c.992C>G
ENST00000673173.1:c.901C>G
ENST00000673451.1:c.1029C>G	ENSP00000500189.1:p.Asp343Glu
ENST00000341594.9:c.24042C>G	ENSP00000341887.6:p.Asp8014Glu
ENST00000347037.9:n.2005C>G
ENST00000354674.4:c.1791C>G	ENSP00000346701.4:p.Asp597Glu
ENST00000367251.7:c.4092C>G	ENSP00000356220.3:p.Asp1364Glu
ENST00000367255.9:c.25257C>G	ENSP00000356224.5:p.Asp8419Glu
ENST00000367256.9:n.8949C>G
ENST00000367257.8:c.3195C>G	ENSP00000356226.4:p.Asp1065Glu
ENST00000409694.6:n.8841C>G
ENST00000423061.5:c.25113C>G	ENSP00000396024.1:p.Asp8371Glu
ENST00000460912.6:n.1871C>G
ENST00000478916.5:n.4279C>G
ENST00000536990.5:n.2094C>G
ENST00000539504.5:c.1722C>G	ENSP00000441052.1:p.Asp574Glu
NM_033071.3:c.25113C>G	NP_149062.1:p.Asp8371Glu
NM_182961.3:c.25257C>G	NP_892006.3:p.Asp8419Glu
XM_006715407.1:c.25362C>G	XP_006715470.1:p.Asp8454Glu
XM_006715408.1:c.25350C>G	XP_006715471.1:p.Asp8450Glu
XM_006715409.1:c.25341C>G	XP_006715472.1:p.Asp8447Glu
XM_006715410.1:c.25362C>G	XP_006715473.1:p.Asp8454Glu
XM_006715411.1:c.25311C>G	XP_006715474.1:p.Asp8437Glu
XM_006715412.1:c.25347C>G	XP_006715475.1:p.Asp8449Glu
XM_006715413.1:c.25293C>G	XP_006715476.1:p.Asp8431Glu
XM_006715414.1:c.25290C>G	XP_006715477.1:p.Asp8430Glu
XM_006715415.1:c.25293C>G	XP_006715478.1:p.Asp8431Glu
XM_006715416.1:c.25278C>G	XP_006715479.1:p.Asp8426Glu
XM_006715417.1:c.25221C>G	XP_006715480.1:p.Asp8407Glu
XM_006715420.1:c.25209C>G	XP_006715483.1:p.Asp8403Glu
XM_006715421.1:c.25206C>G	XP_006715484.1:p.Asp8402Glu
XM_006715422.1:c.25203C>G	XP_006715485.1:p.Asp8401Glu
XM_006715423.1:c.25362C>G	XP_006715486.1:p.Asp8454Glu
XM_006715424.1:c.25362C>G	XP_006715487.1:p.Asp8454Glu
XM_006715425.1:c.25293C>G	XP_006715488.1:p.Asp8431Glu
XM_011535641.1:c.25359C>G	XP_011533943.1:p.Asp8453Glu
XM_011535642.1:c.25347C>G	XP_011533944.1:p.Asp8449Glu
XM_011535643.1:c.25197C>G	XP_011533945.1:p.Asp8399Glu
XM_011535644.1:c.23637C>G	XP_011533946.1:p.Asp7879Glu
XM_011535645.1:c.23130C>G	XP_011533947.1:p.Asp7710Glu
XM_011535647.1:c.18597C>G	XP_011533949.1:p.Asp6199Glu
NM_001347701.1:c.1863C>G	NP_001334630.1:p.Asp621Glu
NM_001347702.1:c.1791C>G	NP_001334631.1:p.Asp597Glu
XM_006715408.2:c.25350C>G	XP_006715471.1:p.Asp8450Glu
XM_006715410.2:c.25362C>G	XP_006715473.1:p.Asp8454Glu
XM_006715412.2:c.25347C>G	XP_006715475.1:p.Asp8449Glu
XM_006715413.2:c.25293C>G	XP_006715476.1:p.Asp8431Glu
XM_006715415.2:c.25293C>G	XP_006715478.1:p.Asp8431Glu
XM_006715416.2:c.25278C>G	XP_006715479.1:p.Asp8426Glu
XM_006715417.2:c.25221C>G	XP_006715480.1:p.Asp8407Glu
XM_006715420.2:c.25209C>G	XP_006715483.1:p.Asp8403Glu
XM_006715421.2:c.25206C>G	XP_006715484.1:p.Asp8402Glu
XM_006715423.2:c.25362C>G	XP_006715486.1:p.Asp8454Glu
XM_006715424.2:c.25362C>G	XP_006715487.1:p.Asp8454Glu
XM_006715425.2:c.25293C>G	XP_006715488.1:p.Asp8431Glu
XM_011535641.2:c.25359C>G	XP_011533943.1:p.Asp8453Glu
XM_011535642.2:c.25347C>G	XP_011533944.1:p.Asp8449Glu
XM_011535645.2:c.23130C>G	XP_011533947.1:p.Asp7710Glu
XM_017010608.1:c.25362C>G	XP_016866097.1:p.Asp8454Glu
XM_017010609.1:c.25362C>G	XP_016866098.1:p.Asp8454Glu
XM_017010610.1:c.25341C>G	XP_016866099.1:p.Asp8447Glu
XM_017010611.2:c.25335C>G	XP_016866100.1:p.Asp8445Glu
XM_017010612.1:c.25284C>G	XP_016866101.1:p.Asp8428Glu
XM_017010613.1:c.25290C>G	XP_016866102.1:p.Asp8430Glu
XM_017010614.1:c.25206C>G	XP_016866103.1:p.Asp8402Glu
XM_017010615.1:c.25137C>G	XP_016866104.1:p.Asp8379Glu
XM_017010616.1:c.25293C>G	XP_016866105.1:p.Asp8431Glu
XM_017010617.1:c.25290C>G	XP_016866106.1:p.Asp8430Glu
XM_017010618.1:c.25278C>G	XP_016866107.1:p.Asp8426Glu
XM_017010619.1:c.23637C>G	XP_016866108.1:p.Asp7879Glu
NM_182961.4:c.25257C>G MANE Select	NP_892006.3:p.Asp8419Glu
NM_001347701.2:c.1863C>G	NP_001334630.1:p.Asp621Glu
NM_001347702.2:c.1791C>G MANE Plus Clinical	NP_001334631.1:p.Asp597Glu
NM_033071.5:c.25113C>G	NP_149062.2:p.Asp8371Glu