Canonical Allele Identifier: CA4052957

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152143651G>A , CM000668.2:g.152143651G>A	GRCh38
NC_000006.11:g.152464786G>A , CM000668.1:g.152464786G>A	GRCh37
NC_000006.10:g.152506479G>A	NCBI36
NG_012855.1:g.498749C>T
NG_012855.2:g.498749C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1625C>T MANE Plus Clinical	ENSP00000346701.4:p.Pro542Leu
ENST00000367255.10:c.25091C>T MANE Select	ENSP00000356224.5:p.Pro8364Leu
ENST00000423061.6:c.24947C>T	ENSP00000396024.1:p.Pro8316Leu
ENST00000672154.1:c.493C>T
ENST00000672169.1:c.826C>T
ENST00000673173.1:c.891-3490C>T
ENST00000673451.1:c.863C>T	ENSP00000500189.1:p.Pro288Leu
ENST00000341594.9:c.23876C>T	ENSP00000341887.6:p.Pro7959Leu
ENST00000347037.9:n.1839C>T
ENST00000354674.4:c.1625C>T	ENSP00000346701.4:p.Pro542Leu
ENST00000367251.7:c.3926C>T	ENSP00000356220.3:p.Pro1309Leu
ENST00000367255.9:c.25091C>T	ENSP00000356224.5:p.Pro8364Leu
ENST00000367256.9:n.8783C>T
ENST00000367257.8:c.3029C>T	ENSP00000356226.4:p.Pro1010Leu
ENST00000409694.6:n.8675C>T
ENST00000423061.5:c.24947C>T	ENSP00000396024.1:p.Pro8316Leu
ENST00000460912.6:n.1705C>T
ENST00000478916.5:n.4113C>T
ENST00000536990.5:n.1928C>T
ENST00000539504.5:c.1556C>T	ENSP00000441052.1:p.Pro519Leu
NM_033071.3:c.24947C>T	NP_149062.1:p.Pro8316Leu
NM_182961.3:c.25091C>T	NP_892006.3:p.Pro8364Leu
XM_006715407.1:c.25196C>T	XP_006715470.1:p.Pro8399Leu
XM_006715408.1:c.25184C>T	XP_006715471.1:p.Pro8395Leu
XM_006715409.1:c.25175C>T	XP_006715472.1:p.Pro8392Leu
XM_006715410.1:c.25196C>T	XP_006715473.1:p.Pro8399Leu
XM_006715411.1:c.25145C>T	XP_006715474.1:p.Pro8382Leu
XM_006715412.1:c.25181C>T	XP_006715475.1:p.Pro8394Leu
XM_006715413.1:c.25127C>T	XP_006715476.1:p.Pro8376Leu
XM_006715414.1:c.25124C>T	XP_006715477.1:p.Pro8375Leu
XM_006715415.1:c.25127C>T	XP_006715478.1:p.Pro8376Leu
XM_006715416.1:c.25112C>T	XP_006715479.1:p.Pro8371Leu
XM_006715417.1:c.25055C>T	XP_006715480.1:p.Pro8352Leu
XM_006715420.1:c.25043C>T	XP_006715483.1:p.Pro8348Leu
XM_006715421.1:c.25040C>T	XP_006715484.1:p.Pro8347Leu
XM_006715422.1:c.25037C>T	XP_006715485.1:p.Pro8346Leu
XM_006715423.1:c.25196C>T	XP_006715486.1:p.Pro8399Leu
XM_006715424.1:c.25196C>T	XP_006715487.1:p.Pro8399Leu
XM_006715425.1:c.25127C>T	XP_006715488.1:p.Pro8376Leu
XM_011535641.1:c.25193C>T	XP_011533943.1:p.Pro8398Leu
XM_011535642.1:c.25181C>T	XP_011533944.1:p.Pro8394Leu
XM_011535643.1:c.25031C>T	XP_011533945.1:p.Pro8344Leu
XM_011535644.1:c.23471C>T	XP_011533946.1:p.Pro7824Leu
XM_011535645.1:c.22964C>T	XP_011533947.1:p.Pro7655Leu
XM_011535647.1:c.18431C>T	XP_011533949.1:p.Pro6144Leu
NM_001347701.1:c.1697C>T	NP_001334630.1:p.Pro566Leu
NM_001347702.1:c.1625C>T	NP_001334631.1:p.Pro542Leu
XM_006715408.2:c.25184C>T	XP_006715471.1:p.Pro8395Leu
XM_006715410.2:c.25196C>T	XP_006715473.1:p.Pro8399Leu
XM_006715412.2:c.25181C>T	XP_006715475.1:p.Pro8394Leu
XM_006715413.2:c.25127C>T	XP_006715476.1:p.Pro8376Leu
XM_006715415.2:c.25127C>T	XP_006715478.1:p.Pro8376Leu
XM_006715416.2:c.25112C>T	XP_006715479.1:p.Pro8371Leu
XM_006715417.2:c.25055C>T	XP_006715480.1:p.Pro8352Leu
XM_006715420.2:c.25043C>T	XP_006715483.1:p.Pro8348Leu
XM_006715421.2:c.25040C>T	XP_006715484.1:p.Pro8347Leu
XM_006715423.2:c.25196C>T	XP_006715486.1:p.Pro8399Leu
XM_006715424.2:c.25196C>T	XP_006715487.1:p.Pro8399Leu
XM_006715425.2:c.25127C>T	XP_006715488.1:p.Pro8376Leu
XM_011535641.2:c.25193C>T	XP_011533943.1:p.Pro8398Leu
XM_011535642.2:c.25181C>T	XP_011533944.1:p.Pro8394Leu
XM_011535645.2:c.22964C>T	XP_011533947.1:p.Pro7655Leu
XM_017010608.1:c.25196C>T	XP_016866097.1:p.Pro8399Leu
XM_017010609.1:c.25196C>T	XP_016866098.1:p.Pro8399Leu
XM_017010610.1:c.25175C>T	XP_016866099.1:p.Pro8392Leu
XM_017010611.2:c.25169C>T	XP_016866100.1:p.Pro8390Leu
XM_017010612.1:c.25118C>T	XP_016866101.1:p.Pro8373Leu
XM_017010613.1:c.25124C>T	XP_016866102.1:p.Pro8375Leu
XM_017010614.1:c.25040C>T	XP_016866103.1:p.Pro8347Leu
XM_017010615.1:c.24971C>T	XP_016866104.1:p.Pro8324Leu
XM_017010616.1:c.25127C>T	XP_016866105.1:p.Pro8376Leu
XM_017010617.1:c.25124C>T	XP_016866106.1:p.Pro8375Leu
XM_017010618.1:c.25112C>T	XP_016866107.1:p.Pro8371Leu
XM_017010619.1:c.23471C>T	XP_016866108.1:p.Pro7824Leu
NM_182961.4:c.25091C>T MANE Select	NP_892006.3:p.Pro8364Leu
NM_001347701.2:c.1697C>T	NP_001334630.1:p.Pro566Leu
NM_001347702.2:c.1625C>T MANE Plus Clinical	NP_001334631.1:p.Pro542Leu
NM_033071.5:c.24947C>T	NP_149062.2:p.Pro8316Leu