Canonical Allele Identifier: CA366079925

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461089A>T (hg19) ; chr6:g.152139954A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152139954A>T , CM000668.2:g.152139954A>T	GRCh38
NC_000006.11:g.152461089A>T , CM000668.1:g.152461089A>T	GRCh37
NC_000006.10:g.152502782A>T	NCBI36
NG_012855.1:g.502446T>A
NG_012855.2:g.502446T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1988T>A MANE Plus Clinical	ENSP00000346701.4:p.Leu663His
ENST00000367255.10:c.25454T>A MANE Select	ENSP00000356224.5:p.Leu8485His
ENST00000423061.6:c.25310T>A	ENSP00000396024.1:p.Leu8437His
ENST00000672154.1:c.856T>A
ENST00000672169.1:c.1189T>A
ENST00000673173.1:c.1098T>A
ENST00000673451.1:c.1226T>A	ENSP00000500189.1:p.Leu409His
ENST00000341594.9:c.24239T>A	ENSP00000341887.6:p.Leu8080His
ENST00000347037.9:n.2202T>A
ENST00000354674.4:c.1988T>A	ENSP00000346701.4:p.Leu663His
ENST00000367251.7:c.4289T>A	ENSP00000356220.3:p.Leu1430His
ENST00000367255.9:c.25454T>A	ENSP00000356224.5:p.Leu8485His
ENST00000367256.9:n.9146T>A
ENST00000367257.8:c.3392T>A	ENSP00000356226.4:p.Leu1131His
ENST00000409694.6:n.9038T>A
ENST00000423061.5:c.25310T>A	ENSP00000396024.1:p.Leu8437His
ENST00000460912.6:n.2068T>A
ENST00000478916.5:n.4476T>A
ENST00000536990.5:n.2291T>A
ENST00000539504.5:c.1919T>A	ENSP00000441052.1:p.Leu640His
NM_033071.3:c.25310T>A	NP_149062.1:p.Leu8437His
NM_182961.3:c.25454T>A	NP_892006.3:p.Leu8485His
XM_006715407.1:c.25559T>A	XP_006715470.1:p.Leu8520His
XM_006715408.1:c.25547T>A	XP_006715471.1:p.Leu8516His
XM_006715409.1:c.25538T>A	XP_006715472.1:p.Leu8513His
XM_006715410.1:c.25559T>A	XP_006715473.1:p.Leu8520His
XM_006715411.1:c.25508T>A	XP_006715474.1:p.Leu8503His
XM_006715412.1:c.25544T>A	XP_006715475.1:p.Leu8515His
XM_006715413.1:c.25490T>A	XP_006715476.1:p.Leu8497His
XM_006715414.1:c.25487T>A	XP_006715477.1:p.Leu8496His
XM_006715415.1:c.25490T>A	XP_006715478.1:p.Leu8497His
XM_006715416.1:c.25475T>A	XP_006715479.1:p.Leu8492His
XM_006715417.1:c.25418T>A	XP_006715480.1:p.Leu8473His
XM_006715420.1:c.25406T>A	XP_006715483.1:p.Leu8469His
XM_006715421.1:c.25403T>A	XP_006715484.1:p.Leu8468His
XM_006715422.1:c.25400T>A	XP_006715485.1:p.Leu8467His
XM_006715423.1:c.25559T>A	XP_006715486.1:p.Leu8520His
XM_006715424.1:c.25559T>A	XP_006715487.1:p.Leu8520His
XM_006715425.1:c.25490T>A	XP_006715488.1:p.Leu8497His
XM_011535641.1:c.25556T>A	XP_011533943.1:p.Leu8519His
XM_011535642.1:c.25544T>A	XP_011533944.1:p.Leu8515His
XM_011535643.1:c.25394T>A	XP_011533945.1:p.Leu8465His
XM_011535644.1:c.23834T>A	XP_011533946.1:p.Leu7945His
XM_011535645.1:c.23327T>A	XP_011533947.1:p.Leu7776His
XM_011535647.1:c.18794T>A	XP_011533949.1:p.Leu6265His
NM_001347701.1:c.2060T>A	NP_001334630.1:p.Leu687His
NM_001347702.1:c.1988T>A	NP_001334631.1:p.Leu663His
XM_006715408.2:c.25547T>A	XP_006715471.1:p.Leu8516His
XM_006715410.2:c.25559T>A	XP_006715473.1:p.Leu8520His
XM_006715412.2:c.25544T>A	XP_006715475.1:p.Leu8515His
XM_006715413.2:c.25490T>A	XP_006715476.1:p.Leu8497His
XM_006715415.2:c.25490T>A	XP_006715478.1:p.Leu8497His
XM_006715416.2:c.25475T>A	XP_006715479.1:p.Leu8492His
XM_006715417.2:c.25418T>A	XP_006715480.1:p.Leu8473His
XM_006715420.2:c.25406T>A	XP_006715483.1:p.Leu8469His
XM_006715421.2:c.25403T>A	XP_006715484.1:p.Leu8468His
XM_006715423.2:c.25559T>A	XP_006715486.1:p.Leu8520His
XM_006715424.2:c.25559T>A	XP_006715487.1:p.Leu8520His
XM_006715425.2:c.25490T>A	XP_006715488.1:p.Leu8497His
XM_011535641.2:c.25556T>A	XP_011533943.1:p.Leu8519His
XM_011535642.2:c.25544T>A	XP_011533944.1:p.Leu8515His
XM_011535645.2:c.23327T>A	XP_011533947.1:p.Leu7776His
XM_017010608.1:c.25559T>A	XP_016866097.1:p.Leu8520His
XM_017010609.1:c.25559T>A	XP_016866098.1:p.Leu8520His
XM_017010610.1:c.25538T>A	XP_016866099.1:p.Leu8513His
XM_017010611.2:c.25532T>A	XP_016866100.1:p.Leu8511His
XM_017010612.1:c.25481T>A	XP_016866101.1:p.Leu8494His
XM_017010613.1:c.25487T>A	XP_016866102.1:p.Leu8496His
XM_017010614.1:c.25403T>A	XP_016866103.1:p.Leu8468His
XM_017010615.1:c.25334T>A	XP_016866104.1:p.Leu8445His
XM_017010616.1:c.25490T>A	XP_016866105.1:p.Leu8497His
XM_017010617.1:c.25487T>A	XP_016866106.1:p.Leu8496His
XM_017010618.1:c.25475T>A	XP_016866107.1:p.Leu8492His
XM_017010619.1:c.23834T>A	XP_016866108.1:p.Leu7945His
NM_182961.4:c.25454T>A MANE Select	NP_892006.3:p.Leu8485His
NM_001347701.2:c.2060T>A	NP_001334630.1:p.Leu687His
NM_001347702.2:c.1988T>A MANE Plus Clinical	NP_001334631.1:p.Leu663His
NM_033071.5:c.25310T>A	NP_149062.2:p.Leu8437His