Canonical Allele Identifier: CA366080863

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461262C>A (hg19) ; chr6:g.152140127C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140127C>A , CM000668.2:g.152140127C>A	GRCh38
NC_000006.11:g.152461262C>A , CM000668.1:g.152461262C>A	GRCh37
NC_000006.10:g.152502955C>A	NCBI36
NG_012855.1:g.502273G>T
NG_012855.2:g.502273G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1815G>T MANE Plus Clinical	ENSP00000346701.4:p.Gln605His
ENST00000367255.10:c.25281G>T MANE Select	ENSP00000356224.5:p.Gln8427His
ENST00000423061.6:c.25137G>T	ENSP00000396024.1:p.Gln8379His
ENST00000672154.1:c.683G>T
ENST00000672169.1:c.1016G>T
ENST00000673173.1:c.925G>T
ENST00000673451.1:c.1053G>T	ENSP00000500189.1:p.Gln351His
ENST00000341594.9:c.24066G>T	ENSP00000341887.6:p.Gln8022His
ENST00000347037.9:n.2029G>T
ENST00000354674.4:c.1815G>T	ENSP00000346701.4:p.Gln605His
ENST00000367251.7:c.4116G>T	ENSP00000356220.3:p.Gln1372His
ENST00000367255.9:c.25281G>T	ENSP00000356224.5:p.Gln8427His
ENST00000367256.9:n.8973G>T
ENST00000367257.8:c.3219G>T	ENSP00000356226.4:p.Gln1073His
ENST00000409694.6:n.8865G>T
ENST00000423061.5:c.25137G>T	ENSP00000396024.1:p.Gln8379His
ENST00000460912.6:n.1895G>T
ENST00000478916.5:n.4303G>T
ENST00000536990.5:n.2118G>T
ENST00000539504.5:c.1746G>T	ENSP00000441052.1:p.Gln582His
NM_033071.3:c.25137G>T	NP_149062.1:p.Gln8379His
NM_182961.3:c.25281G>T	NP_892006.3:p.Gln8427His
XM_006715407.1:c.25386G>T	XP_006715470.1:p.Gln8462His
XM_006715408.1:c.25374G>T	XP_006715471.1:p.Gln8458His
XM_006715409.1:c.25365G>T	XP_006715472.1:p.Gln8455His
XM_006715410.1:c.25386G>T	XP_006715473.1:p.Gln8462His
XM_006715411.1:c.25335G>T	XP_006715474.1:p.Gln8445His
XM_006715412.1:c.25371G>T	XP_006715475.1:p.Gln8457His
XM_006715413.1:c.25317G>T	XP_006715476.1:p.Gln8439His
XM_006715414.1:c.25314G>T	XP_006715477.1:p.Gln8438His
XM_006715415.1:c.25317G>T	XP_006715478.1:p.Gln8439His
XM_006715416.1:c.25302G>T	XP_006715479.1:p.Gln8434His
XM_006715417.1:c.25245G>T	XP_006715480.1:p.Gln8415His
XM_006715420.1:c.25233G>T	XP_006715483.1:p.Gln8411His
XM_006715421.1:c.25230G>T	XP_006715484.1:p.Gln8410His
XM_006715422.1:c.25227G>T	XP_006715485.1:p.Gln8409His
XM_006715423.1:c.25386G>T	XP_006715486.1:p.Gln8462His
XM_006715424.1:c.25386G>T	XP_006715487.1:p.Gln8462His
XM_006715425.1:c.25317G>T	XP_006715488.1:p.Gln8439His
XM_011535641.1:c.25383G>T	XP_011533943.1:p.Gln8461His
XM_011535642.1:c.25371G>T	XP_011533944.1:p.Gln8457His
XM_011535643.1:c.25221G>T	XP_011533945.1:p.Gln8407His
XM_011535644.1:c.23661G>T	XP_011533946.1:p.Gln7887His
XM_011535645.1:c.23154G>T	XP_011533947.1:p.Gln7718His
XM_011535647.1:c.18621G>T	XP_011533949.1:p.Gln6207His
NM_001347701.1:c.1887G>T	NP_001334630.1:p.Gln629His
NM_001347702.1:c.1815G>T	NP_001334631.1:p.Gln605His
XM_006715408.2:c.25374G>T	XP_006715471.1:p.Gln8458His
XM_006715410.2:c.25386G>T	XP_006715473.1:p.Gln8462His
XM_006715412.2:c.25371G>T	XP_006715475.1:p.Gln8457His
XM_006715413.2:c.25317G>T	XP_006715476.1:p.Gln8439His
XM_006715415.2:c.25317G>T	XP_006715478.1:p.Gln8439His
XM_006715416.2:c.25302G>T	XP_006715479.1:p.Gln8434His
XM_006715417.2:c.25245G>T	XP_006715480.1:p.Gln8415His
XM_006715420.2:c.25233G>T	XP_006715483.1:p.Gln8411His
XM_006715421.2:c.25230G>T	XP_006715484.1:p.Gln8410His
XM_006715423.2:c.25386G>T	XP_006715486.1:p.Gln8462His
XM_006715424.2:c.25386G>T	XP_006715487.1:p.Gln8462His
XM_006715425.2:c.25317G>T	XP_006715488.1:p.Gln8439His
XM_011535641.2:c.25383G>T	XP_011533943.1:p.Gln8461His
XM_011535642.2:c.25371G>T	XP_011533944.1:p.Gln8457His
XM_011535645.2:c.23154G>T	XP_011533947.1:p.Gln7718His
XM_017010608.1:c.25386G>T	XP_016866097.1:p.Gln8462His
XM_017010609.1:c.25386G>T	XP_016866098.1:p.Gln8462His
XM_017010610.1:c.25365G>T	XP_016866099.1:p.Gln8455His
XM_017010611.2:c.25359G>T	XP_016866100.1:p.Gln8453His
XM_017010612.1:c.25308G>T	XP_016866101.1:p.Gln8436His
XM_017010613.1:c.25314G>T	XP_016866102.1:p.Gln8438His
XM_017010614.1:c.25230G>T	XP_016866103.1:p.Gln8410His
XM_017010615.1:c.25161G>T	XP_016866104.1:p.Gln8387His
XM_017010616.1:c.25317G>T	XP_016866105.1:p.Gln8439His
XM_017010617.1:c.25314G>T	XP_016866106.1:p.Gln8438His
XM_017010618.1:c.25302G>T	XP_016866107.1:p.Gln8434His
XM_017010619.1:c.23661G>T	XP_016866108.1:p.Gln7887His
NM_182961.4:c.25281G>T MANE Select	NP_892006.3:p.Gln8427His
NM_001347701.2:c.1887G>T	NP_001334630.1:p.Gln629His
NM_001347702.2:c.1815G>T MANE Plus Clinical	NP_001334631.1:p.Gln605His
NM_033071.5:c.25137G>T	NP_149062.2:p.Gln8379His