Canonical Allele Identifier: CA1705426478

Gene: SUN3

Linked Data

• dbSNP Id: rs1789080090

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.47992059_47992071del , CM000669.2:g.47992059_47992071del	GRCh38
NC_000007.13:g.48031656_48031668del , CM000669.1:g.48031656_48031668del	GRCh37
NC_000007.12:g.47998181_47998193del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297325.9:c.861+2246_861+2258del MANE Select	ENSP00000297325.4:n.861+2246_861+2258del
ENST00000297325.8:c.861+2246_861+2258del	ENSP00000297325.4:n.861+2246_861+2258del
ENST00000395572.6:c.861+2246_861+2258del	ENSP00000378939.2:n.861+2246_861+2258del
ENST00000412142.5:c.825+2246_825+2258del	ENSP00000410204.2:n.825+2246_825+2258del
ENST00000412371.5:c.327+2246_327+2258del	ENSP00000406887.1:n.327+2246_327+2258del
ENST00000438771.5:c.562-1024_562-1012del	ENSP00000409077.1:n.562-1024_562-1012del
ENST00000449896.2:c.*689+2246_*689+2258del	ENSP00000395392.2:n.*689+2246_*689+2258de...
ENST00000453071.5:c.632+2246_632+2258del
ENST00000453192.3:c.573+2234_573+2246del	ENSP00000387525.3:n.573+2234_573+2246del
ENST00000473723.5:n.339-1024_339-1012del
NM_001030019.1:c.861+2246_861+2258del	NP_001025190.1:n.861+2246_861+2258del
NM_001284350.1:c.825+2246_825+2258del	NP_001271279.1:n.825+2246_825+2258del
NM_152782.3:c.861+2246_861+2258del	NP_689995.3:n.861+2246_861+2258del
XM_011515252.1:c.882+983_882+995del	XP_011513554.1:n.882+983_882+995del
XM_011515253.1:c.582+983_582+995del	XP_011513555.1:n.582+983_582+995del
XM_017011930.1:c.861+2246_861+2258del	XP_016867419.1:n.861+2246_861+2258del
XR_002956417.1:n.1148+822_1148+834del
NM_001030019.2:c.861+2246_861+2258del MANE Select	NP_001025190.1:n.861+2246_861+2258del
NM_001284350.2:c.825+2246_825+2258del	NP_001271279.1:n.825+2246_825+2258del
NM_152782.4:c.861+2246_861+2258del	NP_689995.3:n.861+2246_861+2258del