Canonical Allele Identifier: CA366080322

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461183C>A (hg19) ; chr6:g.152140048C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140048C>A , CM000668.2:g.152140048C>A	GRCh38
NC_000006.11:g.152461183C>A , CM000668.1:g.152461183C>A	GRCh37
NC_000006.10:g.152502876C>A	NCBI36
NG_012855.1:g.502352G>T
NG_012855.2:g.502352G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1894G>T MANE Plus Clinical	ENSP00000346701.4:p.Ala632Ser
ENST00000367255.10:c.25360G>T MANE Select	ENSP00000356224.5:p.Ala8454Ser
ENST00000423061.6:c.25216G>T	ENSP00000396024.1:p.Ala8406Ser
ENST00000672154.1:c.762G>T
ENST00000672169.1:c.1095G>T
ENST00000673173.1:c.1004G>T
ENST00000673451.1:c.1132G>T	ENSP00000500189.1:p.Ala378Ser
ENST00000341594.9:c.24145G>T	ENSP00000341887.6:p.Ala8049Ser
ENST00000347037.9:n.2108G>T
ENST00000354674.4:c.1894G>T	ENSP00000346701.4:p.Ala632Ser
ENST00000367251.7:c.4195G>T	ENSP00000356220.3:p.Ala1399Ser
ENST00000367255.9:c.25360G>T	ENSP00000356224.5:p.Ala8454Ser
ENST00000367256.9:n.9052G>T
ENST00000367257.8:c.3298G>T	ENSP00000356226.4:p.Ala1100Ser
ENST00000409694.6:n.8944G>T
ENST00000423061.5:c.25216G>T	ENSP00000396024.1:p.Ala8406Ser
ENST00000460912.6:n.1974G>T
ENST00000478916.5:n.4382G>T
ENST00000536990.5:n.2197G>T
ENST00000539504.5:c.1825G>T	ENSP00000441052.1:p.Ala609Ser
NM_033071.3:c.25216G>T	NP_149062.1:p.Ala8406Ser
NM_182961.3:c.25360G>T	NP_892006.3:p.Ala8454Ser
XM_006715407.1:c.25465G>T	XP_006715470.1:p.Ala8489Ser
XM_006715408.1:c.25453G>T	XP_006715471.1:p.Ala8485Ser
XM_006715409.1:c.25444G>T	XP_006715472.1:p.Ala8482Ser
XM_006715410.1:c.25465G>T	XP_006715473.1:p.Ala8489Ser
XM_006715411.1:c.25414G>T	XP_006715474.1:p.Ala8472Ser
XM_006715412.1:c.25450G>T	XP_006715475.1:p.Ala8484Ser
XM_006715413.1:c.25396G>T	XP_006715476.1:p.Ala8466Ser
XM_006715414.1:c.25393G>T	XP_006715477.1:p.Ala8465Ser
XM_006715415.1:c.25396G>T	XP_006715478.1:p.Ala8466Ser
XM_006715416.1:c.25381G>T	XP_006715479.1:p.Ala8461Ser
XM_006715417.1:c.25324G>T	XP_006715480.1:p.Ala8442Ser
XM_006715420.1:c.25312G>T	XP_006715483.1:p.Ala8438Ser
XM_006715421.1:c.25309G>T	XP_006715484.1:p.Ala8437Ser
XM_006715422.1:c.25306G>T	XP_006715485.1:p.Ala8436Ser
XM_006715423.1:c.25465G>T	XP_006715486.1:p.Ala8489Ser
XM_006715424.1:c.25465G>T	XP_006715487.1:p.Ala8489Ser
XM_006715425.1:c.25396G>T	XP_006715488.1:p.Ala8466Ser
XM_011535641.1:c.25462G>T	XP_011533943.1:p.Ala8488Ser
XM_011535642.1:c.25450G>T	XP_011533944.1:p.Ala8484Ser
XM_011535643.1:c.25300G>T	XP_011533945.1:p.Ala8434Ser
XM_011535644.1:c.23740G>T	XP_011533946.1:p.Ala7914Ser
XM_011535645.1:c.23233G>T	XP_011533947.1:p.Ala7745Ser
XM_011535647.1:c.18700G>T	XP_011533949.1:p.Ala6234Ser
NM_001347701.1:c.1966G>T	NP_001334630.1:p.Ala656Ser
NM_001347702.1:c.1894G>T	NP_001334631.1:p.Ala632Ser
XM_006715408.2:c.25453G>T	XP_006715471.1:p.Ala8485Ser
XM_006715410.2:c.25465G>T	XP_006715473.1:p.Ala8489Ser
XM_006715412.2:c.25450G>T	XP_006715475.1:p.Ala8484Ser
XM_006715413.2:c.25396G>T	XP_006715476.1:p.Ala8466Ser
XM_006715415.2:c.25396G>T	XP_006715478.1:p.Ala8466Ser
XM_006715416.2:c.25381G>T	XP_006715479.1:p.Ala8461Ser
XM_006715417.2:c.25324G>T	XP_006715480.1:p.Ala8442Ser
XM_006715420.2:c.25312G>T	XP_006715483.1:p.Ala8438Ser
XM_006715421.2:c.25309G>T	XP_006715484.1:p.Ala8437Ser
XM_006715423.2:c.25465G>T	XP_006715486.1:p.Ala8489Ser
XM_006715424.2:c.25465G>T	XP_006715487.1:p.Ala8489Ser
XM_006715425.2:c.25396G>T	XP_006715488.1:p.Ala8466Ser
XM_011535641.2:c.25462G>T	XP_011533943.1:p.Ala8488Ser
XM_011535642.2:c.25450G>T	XP_011533944.1:p.Ala8484Ser
XM_011535645.2:c.23233G>T	XP_011533947.1:p.Ala7745Ser
XM_017010608.1:c.25465G>T	XP_016866097.1:p.Ala8489Ser
XM_017010609.1:c.25465G>T	XP_016866098.1:p.Ala8489Ser
XM_017010610.1:c.25444G>T	XP_016866099.1:p.Ala8482Ser
XM_017010611.2:c.25438G>T	XP_016866100.1:p.Ala8480Ser
XM_017010612.1:c.25387G>T	XP_016866101.1:p.Ala8463Ser
XM_017010613.1:c.25393G>T	XP_016866102.1:p.Ala8465Ser
XM_017010614.1:c.25309G>T	XP_016866103.1:p.Ala8437Ser
XM_017010615.1:c.25240G>T	XP_016866104.1:p.Ala8414Ser
XM_017010616.1:c.25396G>T	XP_016866105.1:p.Ala8466Ser
XM_017010617.1:c.25393G>T	XP_016866106.1:p.Ala8465Ser
XM_017010618.1:c.25381G>T	XP_016866107.1:p.Ala8461Ser
XM_017010619.1:c.23740G>T	XP_016866108.1:p.Ala7914Ser
NM_182961.4:c.25360G>T MANE Select	NP_892006.3:p.Ala8454Ser
NM_001347701.2:c.1966G>T	NP_001334630.1:p.Ala656Ser
NM_001347702.2:c.1894G>T MANE Plus Clinical	NP_001334631.1:p.Ala632Ser
NM_033071.5:c.25216G>T	NP_149062.2:p.Ala8406Ser