Canonical Allele Identifier: CA366080628

Gene: SYNE1

Linked Data

• MyVariant Identifiers: chr6:g.152461228G>C (hg19) ; chr6:g.152140093G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.152140093G>C , CM000668.2:g.152140093G>C	GRCh38
NC_000006.11:g.152461228G>C , CM000668.1:g.152461228G>C	GRCh37
NC_000006.10:g.152502921G>C	NCBI36
NG_012855.1:g.502307C>G
NG_012855.2:g.502307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354674.5:c.1849C>G MANE Plus Clinical	ENSP00000346701.4:p.Leu617Val
ENST00000367255.10:c.25315C>G MANE Select	ENSP00000356224.5:p.Leu8439Val
ENST00000423061.6:c.25171C>G	ENSP00000396024.1:p.Leu8391Val
ENST00000672154.1:c.717C>G
ENST00000672169.1:c.1050C>G
ENST00000673173.1:c.959C>G
ENST00000673451.1:c.1087C>G	ENSP00000500189.1:p.Leu363Val
ENST00000341594.9:c.24100C>G	ENSP00000341887.6:p.Leu8034Val
ENST00000347037.9:n.2063C>G
ENST00000354674.4:c.1849C>G	ENSP00000346701.4:p.Leu617Val
ENST00000367251.7:c.4150C>G	ENSP00000356220.3:p.Leu1384Val
ENST00000367255.9:c.25315C>G	ENSP00000356224.5:p.Leu8439Val
ENST00000367256.9:n.9007C>G
ENST00000367257.8:c.3253C>G	ENSP00000356226.4:p.Leu1085Val
ENST00000409694.6:n.8899C>G
ENST00000423061.5:c.25171C>G	ENSP00000396024.1:p.Leu8391Val
ENST00000460912.6:n.1929C>G
ENST00000478916.5:n.4337C>G
ENST00000536990.5:n.2152C>G
ENST00000539504.5:c.1780C>G	ENSP00000441052.1:p.Leu594Val
NM_033071.3:c.25171C>G	NP_149062.1:p.Leu8391Val
NM_182961.3:c.25315C>G	NP_892006.3:p.Leu8439Val
XM_006715407.1:c.25420C>G	XP_006715470.1:p.Leu8474Val
XM_006715408.1:c.25408C>G	XP_006715471.1:p.Leu8470Val
XM_006715409.1:c.25399C>G	XP_006715472.1:p.Leu8467Val
XM_006715410.1:c.25420C>G	XP_006715473.1:p.Leu8474Val
XM_006715411.1:c.25369C>G	XP_006715474.1:p.Leu8457Val
XM_006715412.1:c.25405C>G	XP_006715475.1:p.Leu8469Val
XM_006715413.1:c.25351C>G	XP_006715476.1:p.Leu8451Val
XM_006715414.1:c.25348C>G	XP_006715477.1:p.Leu8450Val
XM_006715415.1:c.25351C>G	XP_006715478.1:p.Leu8451Val
XM_006715416.1:c.25336C>G	XP_006715479.1:p.Leu8446Val
XM_006715417.1:c.25279C>G	XP_006715480.1:p.Leu8427Val
XM_006715420.1:c.25267C>G	XP_006715483.1:p.Leu8423Val
XM_006715421.1:c.25264C>G	XP_006715484.1:p.Leu8422Val
XM_006715422.1:c.25261C>G	XP_006715485.1:p.Leu8421Val
XM_006715423.1:c.25420C>G	XP_006715486.1:p.Leu8474Val
XM_006715424.1:c.25420C>G	XP_006715487.1:p.Leu8474Val
XM_006715425.1:c.25351C>G	XP_006715488.1:p.Leu8451Val
XM_011535641.1:c.25417C>G	XP_011533943.1:p.Leu8473Val
XM_011535642.1:c.25405C>G	XP_011533944.1:p.Leu8469Val
XM_011535643.1:c.25255C>G	XP_011533945.1:p.Leu8419Val
XM_011535644.1:c.23695C>G	XP_011533946.1:p.Leu7899Val
XM_011535645.1:c.23188C>G	XP_011533947.1:p.Leu7730Val
XM_011535647.1:c.18655C>G	XP_011533949.1:p.Leu6219Val
NM_001347701.1:c.1921C>G	NP_001334630.1:p.Leu641Val
NM_001347702.1:c.1849C>G	NP_001334631.1:p.Leu617Val
XM_006715408.2:c.25408C>G	XP_006715471.1:p.Leu8470Val
XM_006715410.2:c.25420C>G	XP_006715473.1:p.Leu8474Val
XM_006715412.2:c.25405C>G	XP_006715475.1:p.Leu8469Val
XM_006715413.2:c.25351C>G	XP_006715476.1:p.Leu8451Val
XM_006715415.2:c.25351C>G	XP_006715478.1:p.Leu8451Val
XM_006715416.2:c.25336C>G	XP_006715479.1:p.Leu8446Val
XM_006715417.2:c.25279C>G	XP_006715480.1:p.Leu8427Val
XM_006715420.2:c.25267C>G	XP_006715483.1:p.Leu8423Val
XM_006715421.2:c.25264C>G	XP_006715484.1:p.Leu8422Val
XM_006715423.2:c.25420C>G	XP_006715486.1:p.Leu8474Val
XM_006715424.2:c.25420C>G	XP_006715487.1:p.Leu8474Val
XM_006715425.2:c.25351C>G	XP_006715488.1:p.Leu8451Val
XM_011535641.2:c.25417C>G	XP_011533943.1:p.Leu8473Val
XM_011535642.2:c.25405C>G	XP_011533944.1:p.Leu8469Val
XM_011535645.2:c.23188C>G	XP_011533947.1:p.Leu7730Val
XM_017010608.1:c.25420C>G	XP_016866097.1:p.Leu8474Val
XM_017010609.1:c.25420C>G	XP_016866098.1:p.Leu8474Val
XM_017010610.1:c.25399C>G	XP_016866099.1:p.Leu8467Val
XM_017010611.2:c.25393C>G	XP_016866100.1:p.Leu8465Val
XM_017010612.1:c.25342C>G	XP_016866101.1:p.Leu8448Val
XM_017010613.1:c.25348C>G	XP_016866102.1:p.Leu8450Val
XM_017010614.1:c.25264C>G	XP_016866103.1:p.Leu8422Val
XM_017010615.1:c.25195C>G	XP_016866104.1:p.Leu8399Val
XM_017010616.1:c.25351C>G	XP_016866105.1:p.Leu8451Val
XM_017010617.1:c.25348C>G	XP_016866106.1:p.Leu8450Val
XM_017010618.1:c.25336C>G	XP_016866107.1:p.Leu8446Val
XM_017010619.1:c.23695C>G	XP_016866108.1:p.Leu7899Val
NM_182961.4:c.25315C>G MANE Select	NP_892006.3:p.Leu8439Val
NM_001347701.2:c.1921C>G	NP_001334630.1:p.Leu641Val
NM_001347702.2:c.1849C>G MANE Plus Clinical	NP_001334631.1:p.Leu617Val
NM_033071.5:c.25171C>G	NP_149062.2:p.Leu8391Val