Canonical Allele Identifier: CA2156454313
Gene: SYNE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95425866C= , CM000676.2:g.95425866C= GRCh38
NC_000014.8:g.95892203C= , CM000676.1:g.95892203C= GRCh37
NC_000014.7:g.94961956C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000682763.1:c.2727+6213G= MANE Select ENSP00000507501.1:n.2727+6213G=
ENST00000334258.9:c.2727+6213G= ENSP00000334308.4:n.2727+6213G=
ENST00000554873.5:c.1998+6213G= ENSP00000452154.1:n.1998+6213G=
ENST00000557275.5:c.2712+6213G= ENSP00000450562.1:n.2712+6213G=
NM_152592.3:c.2727+6213G= NP_689805.3:n.2727+6213G=
XM_005267376.3:c.2916+6213G= XP_005267433.2:n.2916+6213G=
XM_005267377.2:c.2727+6213G= XP_005267434.1:n.2727+6213G=
XM_006720063.2:c.2727+6213G= XP_006720126.1:n.2727+6213G=
XM_011536513.1:c.2901+6213G= XP_011534815.1:n.2901+6213G=
XM_011536514.1:c.2916+6213G= XP_011534816.1:n.2916+6213G=
XM_011536515.1:c.2751+6213G= XP_011534817.1:n.2751+6213G=
NM_001363692.1:c.2712+6213G= NP_001350621.1:n.2712+6213G=
NM_152592.5:c.2727+6213G= NP_689805.3:n.2727+6213G=
XM_005267377.4:c.2727+6213G= XP_005267434.1:n.2727+6213G=
XM_006720063.4:c.2727+6213G= XP_006720126.1:n.2727+6213G=
XM_011536515.3:c.2751+6213G= XP_011534817.1:n.2751+6213G=
NM_001363692.2:c.2712+6213G= NP_001350621.1:n.2712+6213G=
NM_152592.6:c.2727+6213G= MANE Select NP_689805.3:n.2727+6213G=