Canonical Allele Identifier: CA1705426508
Gene: SUN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.47992096A= , CM000669.2:g.47992096A= GRCh38
NC_000007.13:g.48031693A= , CM000669.1:g.48031693A= GRCh37
NC_000007.12:g.47998218A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297325.9:c.861+2219T= MANE Select ENSP00000297325.4:n.861+2219T=
ENST00000297325.8:c.861+2219T= ENSP00000297325.4:n.861+2219T=
ENST00000395572.6:c.861+2219T= ENSP00000378939.2:n.861+2219T=
ENST00000412142.5:c.825+2219T= ENSP00000410204.2:n.825+2219T=
ENST00000412371.5:c.327+2219T= ENSP00000406887.1:n.327+2219T=
ENST00000438771.5:c.562-1051T= ENSP00000409077.1:n.562-1051T=
ENST00000449896.2:c.*689+2219T= ENSP00000395392.2:n.*689+2219T=
ENST00000453071.5:c.632+2219T=
ENST00000453192.3:c.573+2207T= ENSP00000387525.3:n.573+2207T=
ENST00000473723.5:n.339-1051T=
NM_001030019.1:c.861+2219T= NP_001025190.1:n.861+2219T=
NM_001284350.1:c.825+2219T= NP_001271279.1:n.825+2219T=
NM_152782.3:c.861+2219T= NP_689995.3:n.861+2219T=
XM_011515252.1:c.882+956T= XP_011513554.1:n.882+956T=
XM_011515253.1:c.582+956T= XP_011513555.1:n.582+956T=
XM_017011930.1:c.861+2219T= XP_016867419.1:n.861+2219T=
XR_002956417.1:n.1148+795T=
NM_001030019.2:c.861+2219T= MANE Select NP_001025190.1:n.861+2219T=
NM_001284350.2:c.825+2219T= NP_001271279.1:n.825+2219T=
NM_152782.4:c.861+2219T= NP_689995.3:n.861+2219T=