Canonical Allele Identifier: CA1705426492
Gene: SUN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.47992079G= , CM000669.2:g.47992079G= GRCh38
NC_000007.13:g.48031676G= , CM000669.1:g.48031676G= GRCh37
NC_000007.12:g.47998201G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297325.9:c.861+2236C= MANE Select ENSP00000297325.4:n.861+2236C=
ENST00000297325.8:c.861+2236C= ENSP00000297325.4:n.861+2236C=
ENST00000395572.6:c.861+2236C= ENSP00000378939.2:n.861+2236C=
ENST00000412142.5:c.825+2236C= ENSP00000410204.2:n.825+2236C=
ENST00000412371.5:c.327+2236C= ENSP00000406887.1:n.327+2236C=
ENST00000438771.5:c.562-1034C= ENSP00000409077.1:n.562-1034C=
ENST00000449896.2:c.*689+2236C= ENSP00000395392.2:n.*689+2236C=
ENST00000453071.5:c.632+2236C=
ENST00000453192.3:c.573+2224C= ENSP00000387525.3:n.573+2224C=
ENST00000473723.5:n.339-1034C=
NM_001030019.1:c.861+2236C= NP_001025190.1:n.861+2236C=
NM_001284350.1:c.825+2236C= NP_001271279.1:n.825+2236C=
NM_152782.3:c.861+2236C= NP_689995.3:n.861+2236C=
XM_011515252.1:c.882+973C= XP_011513554.1:n.882+973C=
XM_011515253.1:c.582+973C= XP_011513555.1:n.582+973C=
XM_017011930.1:c.861+2236C= XP_016867419.1:n.861+2236C=
XR_002956417.1:n.1148+812C=
NM_001030019.2:c.861+2236C= MANE Select NP_001025190.1:n.861+2236C=
NM_001284350.2:c.825+2236C= NP_001271279.1:n.825+2236C=
NM_152782.4:c.861+2236C= NP_689995.3:n.861+2236C=