Canonical Allele Identifier: CA1673206327

Gene: SYNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140066C= , CM000668.2:g.152140066C=	GRCh38
NC_000006.11:g.152461201C= , CM000668.1:g.152461201C=	GRCh37
NC_000006.10:g.152502894C=	NCBI36
NG_012855.1:g.502334G=
NG_012855.2:g.502334G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1876G= MANE Plus Clinical	ENSP00000346701.4:p.Asp626=
ENST00000367255.10:c.25342G= MANE Select	ENSP00000356224.5:p.Asp8448=
ENST00000423061.6:c.25198G=	ENSP00000396024.1:p.Asp8400=
ENST00000672154.1:c.744G=
ENST00000672169.1:c.1077G=
ENST00000673173.1:c.986G=
ENST00000673451.1:c.1114G=	ENSP00000500189.1:p.Asp372=
ENST00000341594.9:c.24127G=	ENSP00000341887.6:p.Asp8043=
ENST00000347037.9:n.2090G=
ENST00000354674.4:c.1876G=	ENSP00000346701.4:p.Asp626=
ENST00000367251.7:c.4177G=	ENSP00000356220.3:p.Asp1393=
ENST00000367255.9:c.25342G=	ENSP00000356224.5:p.Asp8448=
ENST00000367256.9:n.9034G=
ENST00000367257.8:c.3280G=	ENSP00000356226.4:p.Asp1094=
ENST00000409694.6:n.8926G=
ENST00000423061.5:c.25198G=	ENSP00000396024.1:p.Asp8400=
ENST00000460912.6:n.1956G=
ENST00000478916.5:n.4364G=
ENST00000536990.5:n.2179G=
ENST00000539504.5:c.1807G=	ENSP00000441052.1:p.Asp603=
NM_033071.3:c.25198G=	NP_149062.1:p.Asp8400=
NM_182961.3:c.25342G=	NP_892006.3:p.Asp8448=
XM_006715407.1:c.25447G=	XP_006715470.1:p.Asp8483=
XM_006715408.1:c.25435G=	XP_006715471.1:p.Asp8479=
XM_006715409.1:c.25426G=	XP_006715472.1:p.Asp8476=
XM_006715410.1:c.25447G=	XP_006715473.1:p.Asp8483=
XM_006715411.1:c.25396G=	XP_006715474.1:p.Asp8466=
XM_006715412.1:c.25432G=	XP_006715475.1:p.Asp8478=
XM_006715413.1:c.25378G=	XP_006715476.1:p.Asp8460=
XM_006715414.1:c.25375G=	XP_006715477.1:p.Asp8459=
XM_006715415.1:c.25378G=	XP_006715478.1:p.Asp8460=
XM_006715416.1:c.25363G=	XP_006715479.1:p.Asp8455=
XM_006715417.1:c.25306G=	XP_006715480.1:p.Asp8436=
XM_006715420.1:c.25294G=	XP_006715483.1:p.Asp8432=
XM_006715421.1:c.25291G=	XP_006715484.1:p.Asp8431=
XM_006715422.1:c.25288G=	XP_006715485.1:p.Asp8430=
XM_006715423.1:c.25447G=	XP_006715486.1:p.Asp8483=
XM_006715424.1:c.25447G=	XP_006715487.1:p.Asp8483=
XM_006715425.1:c.25378G=	XP_006715488.1:p.Asp8460=
XM_011535641.1:c.25444G=	XP_011533943.1:p.Asp8482=
XM_011535642.1:c.25432G=	XP_011533944.1:p.Asp8478=
XM_011535643.1:c.25282G=	XP_011533945.1:p.Asp8428=
XM_011535644.1:c.23722G=	XP_011533946.1:p.Asp7908=
XM_011535645.1:c.23215G=	XP_011533947.1:p.Asp7739=
XM_011535647.1:c.18682G=	XP_011533949.1:p.Asp6228=
NM_001347701.1:c.1948G=	NP_001334630.1:p.Asp650=
NM_001347702.1:c.1876G=	NP_001334631.1:p.Asp626=
XM_006715408.2:c.25435G=	XP_006715471.1:p.Asp8479=
XM_006715410.2:c.25447G=	XP_006715473.1:p.Asp8483=
XM_006715412.2:c.25432G=	XP_006715475.1:p.Asp8478=
XM_006715413.2:c.25378G=	XP_006715476.1:p.Asp8460=
XM_006715415.2:c.25378G=	XP_006715478.1:p.Asp8460=
XM_006715416.2:c.25363G=	XP_006715479.1:p.Asp8455=
XM_006715417.2:c.25306G=	XP_006715480.1:p.Asp8436=
XM_006715420.2:c.25294G=	XP_006715483.1:p.Asp8432=
XM_006715421.2:c.25291G=	XP_006715484.1:p.Asp8431=
XM_006715423.2:c.25447G=	XP_006715486.1:p.Asp8483=
XM_006715424.2:c.25447G=	XP_006715487.1:p.Asp8483=
XM_006715425.2:c.25378G=	XP_006715488.1:p.Asp8460=
XM_011535641.2:c.25444G=	XP_011533943.1:p.Asp8482=
XM_011535642.2:c.25432G=	XP_011533944.1:p.Asp8478=
XM_011535645.2:c.23215G=	XP_011533947.1:p.Asp7739=
XM_017010608.1:c.25447G=	XP_016866097.1:p.Asp8483=
XM_017010609.1:c.25447G=	XP_016866098.1:p.Asp8483=
XM_017010610.1:c.25426G=	XP_016866099.1:p.Asp8476=
XM_017010611.2:c.25420G=	XP_016866100.1:p.Asp8474=
XM_017010612.1:c.25369G=	XP_016866101.1:p.Asp8457=
XM_017010613.1:c.25375G=	XP_016866102.1:p.Asp8459=
XM_017010614.1:c.25291G=	XP_016866103.1:p.Asp8431=
XM_017010615.1:c.25222G=	XP_016866104.1:p.Asp8408=
XM_017010616.1:c.25378G=	XP_016866105.1:p.Asp8460=
XM_017010617.1:c.25375G=	XP_016866106.1:p.Asp8459=
XM_017010618.1:c.25363G=	XP_016866107.1:p.Asp8455=
XM_017010619.1:c.23722G=	XP_016866108.1:p.Asp7908=
NM_182961.4:c.25342G= MANE Select	NP_892006.3:p.Asp8448=
NM_001347701.2:c.1948G=	NP_001334630.1:p.Asp650=
NM_001347702.2:c.1876G= MANE Plus Clinical	NP_001334631.1:p.Asp626=
NM_033071.5:c.25198G=	NP_149062.2:p.Asp8400=