Canonical Allele Identifier: CA4058839
Community Standard Title: NM_182961.4(SYNE1):c.3465C>T (p.Ile1155=)
Gene: SYNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152449572G>A , CM000668.2:g.152449572G>A GRCh38
NC_000006.11:g.152770707G>A , CM000668.1:g.152770707G>A GRCh37
NC_000006.10:g.152812400G>A NCBI36
NG_012855.1:g.192828C>T
NG_012855.2:g.192828C>T

Transcript Alleles

HGVS Amino-acid Change
NM_182961.4:c.3465C>T MANE Select NP_892006.3:p.Ile1155=
ENST00000367255.10:c.3465C>T MANE Select ENSP00000356224.5:p.Ile1155=
NM_033071.3:c.3486C>T NP_149062.1:p.Ile1162=
NM_033071.5:c.3486C>T NP_149062.2:p.Ile1162=
NM_182961.3:c.3465C>T NP_892006.3:p.Ile1155=
ENST00000341594.9:c.3612C>T ENSP00000341887.6:p.Ile1204=
ENST00000367248.7:c.3435C>T ENSP00000356217.3:p.Ile1145=
ENST00000367253.8:c.3465C>T ENSP00000356222.4:p.Ile1155=
ENST00000367255.9:c.3465C>T ENSP00000356224.5:p.Ile1155=
ENST00000413186.6:c.3465C>T ENSP00000414510.2:p.Ile1155=
ENST00000423061.5:c.3486C>T ENSP00000396024.1:p.Ile1162=
ENST00000423061.6:c.3486C>T ENSP00000396024.1:p.Ile1162=
ENST00000461872.6:n.3683C>T
ENST00000671915.1:c.762C>T ENSP00000500319.1:p.Ile254=
ENST00000672122.1:c.3408C>T ENSP00000500559.1:p.Ile1136=
ENST00000673163.1:c.*3435C>T ENSP00000499934.1:n.*3435C>T
ENST00000673281.1:c.3459C>T ENSP00000500893.1:p.Ile1153=
XM_006715407.1:c.3486C>T XP_006715470.1:p.Ile1162=
XM_006715408.1:c.3486C>T XP_006715471.1:p.Ile1162=
XM_006715408.2:c.3486C>T XP_006715471.1:p.Ile1162=
XM_006715409.1:c.3465C>T XP_006715472.1:p.Ile1155=
XM_006715410.1:c.3486C>T XP_006715473.1:p.Ile1162=
XM_006715410.2:c.3486C>T XP_006715473.1:p.Ile1162=
XM_006715411.1:c.3435C>T XP_006715474.1:p.Ile1145=
XM_006715412.1:c.3486C>T XP_006715475.1:p.Ile1162=
XM_006715412.2:c.3486C>T XP_006715475.1:p.Ile1162=
XM_006715413.1:c.3486C>T XP_006715476.1:p.Ile1162=
XM_006715413.2:c.3486C>T XP_006715476.1:p.Ile1162=
XM_006715414.1:c.3414C>T XP_006715477.1:p.Ile1138=
XM_006715415.1:c.3486C>T XP_006715478.1:p.Ile1162=
XM_006715415.2:c.3486C>T XP_006715478.1:p.Ile1162=
XM_006715416.1:c.3486C>T XP_006715479.1:p.Ile1162=
XM_006715416.2:c.3486C>T XP_006715479.1:p.Ile1162=
XM_006715417.1:c.3486C>T XP_006715480.1:p.Ile1162=
XM_006715417.2:c.3486C>T XP_006715480.1:p.Ile1162=
XM_006715420.1:c.3486C>T XP_006715483.1:p.Ile1162=
XM_006715420.2:c.3486C>T XP_006715483.1:p.Ile1162=
XM_006715421.1:c.3486C>T XP_006715484.1:p.Ile1162=
XM_006715421.2:c.3486C>T XP_006715484.1:p.Ile1162=
XM_006715422.1:c.3327C>T XP_006715485.1:p.Ile1109=
XM_006715423.1:c.3486C>T XP_006715486.1:p.Ile1162=
XM_006715423.2:c.3486C>T XP_006715486.1:p.Ile1162=
XM_006715424.1:c.3486C>T XP_006715487.1:p.Ile1162=
XM_006715424.2:c.3486C>T XP_006715487.1:p.Ile1162=
XM_006715425.1:c.3486C>T XP_006715488.1:p.Ile1162=
XM_006715425.2:c.3486C>T XP_006715488.1:p.Ile1162=
XM_011535641.1:c.3486C>T XP_011533943.1:p.Ile1162=
XM_011535641.2:c.3486C>T XP_011533943.1:p.Ile1162=
XM_011535642.1:c.3486C>T XP_011533944.1:p.Ile1162=
XM_011535642.2:c.3486C>T XP_011533944.1:p.Ile1162=
XM_011535643.1:c.3321C>T XP_011533945.1:p.Ile1107=
XM_011535644.1:c.1761C>T XP_011533946.1:p.Ile587=
XM_011535645.1:c.1254C>T XP_011533947.1:p.Ile418=
XM_011535645.2:c.1254C>T XP_011533947.1:p.Ile418=
XM_011535646.1:c.3486C>T XP_011533948.1:p.Ile1162=
XM_017010608.1:c.3486C>T XP_016866097.1:p.Ile1162=
XM_017010609.1:c.3486C>T XP_016866098.1:p.Ile1162=
XM_017010610.1:c.3465C>T XP_016866099.1:p.Ile1155=
XM_017010611.2:c.3459C>T XP_016866100.1:p.Ile1153=
XM_017010612.1:c.3408C>T XP_016866101.1:p.Ile1136=
XM_017010613.1:c.3486C>T XP_016866102.1:p.Ile1162=
XM_017010614.1:c.3486C>T XP_016866103.1:p.Ile1162=
XM_017010615.1:c.3486C>T XP_016866104.1:p.Ile1162=
XM_017010616.1:c.3486C>T XP_016866105.1:p.Ile1162=
XM_017010617.1:c.3486C>T XP_016866106.1:p.Ile1162=
XM_017010618.1:c.3486C>T XP_016866107.1:p.Ile1162=
XM_017010619.1:c.1761C>T XP_016866108.1:p.Ile587=
XR_001743287.1:n.3969C>T