Canonical Allele Identifier: CA507317050
Gene: SYNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.36497391C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36006489C>G , CM000681.2:g.36006489C>G GRCh38
NC_000019.9:g.36497391C>G , CM000681.1:g.36497391C>G GRCh37
NC_000019.8:g.41189231C>G NCBI36
NG_042831.1:g.7305G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324444.9:c.801G>C MANE Select ENSP00000316130.3:p.Arg267=
ENST00000397428.8:c.67-1052G>C
ENST00000465425.2:n.913G>C
ENST00000324444.7:c.801G>C ENSP00000316130.3:p.Arg267=
ENST00000340477.9:c.462G>C ENSP00000343152.5:p.Arg154=
ENST00000397428.7:c.40-1052G>C ENSP00000380572.3:n.40-1052G>C
ENST00000465425.1:n.913G>C
ENST00000490730.1:c.688+113G>C ENSP00000422716.1:n.688+113G>C
ENST00000503121.5:c.242+1728G>C
ENST00000505054.2:n.395-1052G>C
NM_001039876.1:c.801G>C NP_001034965.1:p.Arg267=
NM_001039876.2:c.801G>C NP_001034965.1:p.Arg267=
NM_001297735.1:c.462G>C NP_001284664.1:p.Arg154=
NM_001297735.2:c.462G>C NP_001284664.1:p.Arg154=
XM_005258598.2:c.688+113G>C XP_005258655.1:n.688+113G>C
XM_005258601.2:c.618+261G>C XP_005258658.1:n.618+261G>C
XM_005258604.3:c.688+113G>C XP_005258661.1:n.688+113G>C
NM_001039876.3:c.801G>C MANE Select NP_001034965.1:p.Arg267=
NM_001297735.3:c.462G>C NP_001284664.1:p.Arg154=