Canonical Allele Identifier: CA366083305

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152464880A>G (hg19) ; chr6:g.152143745A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152143745A>G , CM000668.2:g.152143745A>G	GRCh38
NC_000006.11:g.152464880A>G , CM000668.1:g.152464880A>G	GRCh37
NC_000006.10:g.152506573A>G	NCBI36
NG_012855.1:g.498655T>C
NG_012855.2:g.498655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1531T>C MANE Plus Clinical	ENSP00000346701.4:p.Ser511Pro
ENST00000367255.10:c.24997T>C MANE Select	ENSP00000356224.5:p.Ser8333Pro
ENST00000423061.6:c.24853T>C	ENSP00000396024.1:p.Ser8285Pro
ENST00000672154.1:c.399T>C
ENST00000672169.1:c.732T>C
ENST00000673173.1:c.891-3584T>C
ENST00000673451.1:c.769T>C	ENSP00000500189.1:p.Ser257Pro
ENST00000341594.9:c.23782T>C	ENSP00000341887.6:p.Ser7928Pro
ENST00000347037.9:n.1745T>C
ENST00000354674.4:c.1531T>C	ENSP00000346701.4:p.Ser511Pro
ENST00000367251.7:c.3832T>C	ENSP00000356220.3:p.Ser1278Pro
ENST00000367255.9:c.24997T>C	ENSP00000356224.5:p.Ser8333Pro
ENST00000367256.9:n.8689T>C
ENST00000367257.8:c.2935T>C	ENSP00000356226.4:p.Ser979Pro
ENST00000409694.6:n.8581T>C
ENST00000423061.5:c.24853T>C	ENSP00000396024.1:p.Ser8285Pro
ENST00000460912.6:n.1611T>C
ENST00000478916.5:n.4019T>C
ENST00000536990.5:n.1834T>C
ENST00000539504.5:c.1462T>C	ENSP00000441052.1:p.Ser488Pro
NM_033071.3:c.24853T>C	NP_149062.1:p.Ser8285Pro
NM_182961.3:c.24997T>C	NP_892006.3:p.Ser8333Pro
XM_006715407.1:c.25102T>C	XP_006715470.1:p.Ser8368Pro
XM_006715408.1:c.25090T>C	XP_006715471.1:p.Ser8364Pro
XM_006715409.1:c.25081T>C	XP_006715472.1:p.Ser8361Pro
XM_006715410.1:c.25102T>C	XP_006715473.1:p.Ser8368Pro
XM_006715411.1:c.25051T>C	XP_006715474.1:p.Ser8351Pro
XM_006715412.1:c.25087T>C	XP_006715475.1:p.Ser8363Pro
XM_006715413.1:c.25033T>C	XP_006715476.1:p.Ser8345Pro
XM_006715414.1:c.25030T>C	XP_006715477.1:p.Ser8344Pro
XM_006715415.1:c.25033T>C	XP_006715478.1:p.Ser8345Pro
XM_006715416.1:c.25018T>C	XP_006715479.1:p.Ser8340Pro
XM_006715417.1:c.24961T>C	XP_006715480.1:p.Ser8321Pro
XM_006715420.1:c.24949T>C	XP_006715483.1:p.Ser8317Pro
XM_006715421.1:c.24946T>C	XP_006715484.1:p.Ser8316Pro
XM_006715422.1:c.24943T>C	XP_006715485.1:p.Ser8315Pro
XM_006715423.1:c.25102T>C	XP_006715486.1:p.Ser8368Pro
XM_006715424.1:c.25102T>C	XP_006715487.1:p.Ser8368Pro
XM_006715425.1:c.25033T>C	XP_006715488.1:p.Ser8345Pro
XM_011535641.1:c.25099T>C	XP_011533943.1:p.Ser8367Pro
XM_011535642.1:c.25087T>C	XP_011533944.1:p.Ser8363Pro
XM_011535643.1:c.24937T>C	XP_011533945.1:p.Ser8313Pro
XM_011535644.1:c.23377T>C	XP_011533946.1:p.Ser7793Pro
XM_011535645.1:c.22870T>C	XP_011533947.1:p.Ser7624Pro
XM_011535647.1:c.18337T>C	XP_011533949.1:p.Ser6113Pro
NM_001347701.1:c.1603T>C	NP_001334630.1:p.Ser535Pro
NM_001347702.1:c.1531T>C	NP_001334631.1:p.Ser511Pro
XM_006715408.2:c.25090T>C	XP_006715471.1:p.Ser8364Pro
XM_006715410.2:c.25102T>C	XP_006715473.1:p.Ser8368Pro
XM_006715412.2:c.25087T>C	XP_006715475.1:p.Ser8363Pro
XM_006715413.2:c.25033T>C	XP_006715476.1:p.Ser8345Pro
XM_006715415.2:c.25033T>C	XP_006715478.1:p.Ser8345Pro
XM_006715416.2:c.25018T>C	XP_006715479.1:p.Ser8340Pro
XM_006715417.2:c.24961T>C	XP_006715480.1:p.Ser8321Pro
XM_006715420.2:c.24949T>C	XP_006715483.1:p.Ser8317Pro
XM_006715421.2:c.24946T>C	XP_006715484.1:p.Ser8316Pro
XM_006715423.2:c.25102T>C	XP_006715486.1:p.Ser8368Pro
XM_006715424.2:c.25102T>C	XP_006715487.1:p.Ser8368Pro
XM_006715425.2:c.25033T>C	XP_006715488.1:p.Ser8345Pro
XM_011535641.2:c.25099T>C	XP_011533943.1:p.Ser8367Pro
XM_011535642.2:c.25087T>C	XP_011533944.1:p.Ser8363Pro
XM_011535645.2:c.22870T>C	XP_011533947.1:p.Ser7624Pro
XM_017010608.1:c.25102T>C	XP_016866097.1:p.Ser8368Pro
XM_017010609.1:c.25102T>C	XP_016866098.1:p.Ser8368Pro
XM_017010610.1:c.25081T>C	XP_016866099.1:p.Ser8361Pro
XM_017010611.2:c.25075T>C	XP_016866100.1:p.Ser8359Pro
XM_017010612.1:c.25024T>C	XP_016866101.1:p.Ser8342Pro
XM_017010613.1:c.25030T>C	XP_016866102.1:p.Ser8344Pro
XM_017010614.1:c.24946T>C	XP_016866103.1:p.Ser8316Pro
XM_017010615.1:c.24877T>C	XP_016866104.1:p.Ser8293Pro
XM_017010616.1:c.25033T>C	XP_016866105.1:p.Ser8345Pro
XM_017010617.1:c.25030T>C	XP_016866106.1:p.Ser8344Pro
XM_017010618.1:c.25018T>C	XP_016866107.1:p.Ser8340Pro
XM_017010619.1:c.23377T>C	XP_016866108.1:p.Ser7793Pro
NM_182961.4:c.24997T>C MANE Select	NP_892006.3:p.Ser8333Pro
NM_001347701.2:c.1603T>C	NP_001334630.1:p.Ser535Pro
NM_001347702.2:c.1531T>C MANE Plus Clinical	NP_001334631.1:p.Ser511Pro
NM_033071.5:c.24853T>C	NP_149062.2:p.Ser8285Pro