Canonical Allele Identifier: CA2775332275
Gene: SUN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.47992076_47992083dup , CM000669.2:g.47992076_47992083dup GRCh38
NC_000007.13:g.48031673_48031680dup , CM000669.1:g.48031673_48031680dup GRCh37
NC_000007.12:g.47998198_47998205dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297325.9:c.861+2234_861+2241dup MANE Select ENSP00000297325.4:n.861+2234_861+2241dup
ENST00000297325.8:c.861+2234_861+2241dup ENSP00000297325.4:n.861+2234_861+2241dup
ENST00000395572.6:c.861+2234_861+2241dup ENSP00000378939.2:n.861+2234_861+2241dup
ENST00000412142.5:c.825+2234_825+2241dup ENSP00000410204.2:n.825+2234_825+2241dup
ENST00000412371.5:c.327+2234_327+2241dup ENSP00000406887.1:n.327+2234_327+2241dup
ENST00000438771.5:c.562-1036_562-1029dup ENSP00000409077.1:n.562-1036_562-1029dup
ENST00000449896.2:c.*689+2234_*689+2241dup ENSP00000395392.2:n.*689+2234_*689+2241dup
ENST00000453071.5:c.632+2234_632+2241dup
ENST00000453192.3:c.573+2222_573+2229dup ENSP00000387525.3:n.573+2222_573+2229dup
ENST00000473723.5:n.339-1036_339-1029dup
NM_001030019.1:c.861+2234_861+2241dup NP_001025190.1:n.861+2234_861+2241dup
NM_001284350.1:c.825+2234_825+2241dup NP_001271279.1:n.825+2234_825+2241dup
NM_152782.3:c.861+2234_861+2241dup NP_689995.3:n.861+2234_861+2241dup
XM_011515252.1:c.882+971_882+978dup XP_011513554.1:n.882+971_882+978dup
XM_011515253.1:c.582+971_582+978dup XP_011513555.1:n.582+971_582+978dup
XM_017011930.1:c.861+2234_861+2241dup XP_016867419.1:n.861+2234_861+2241dup
XR_002956417.1:n.1148+810_1148+817dup
NM_001030019.2:c.861+2234_861+2241dup MANE Select NP_001025190.1:n.861+2234_861+2241dup
NM_001284350.2:c.825+2234_825+2241dup NP_001271279.1:n.825+2234_825+2241dup
NM_152782.4:c.861+2234_861+2241dup NP_689995.3:n.861+2234_861+2241dup