Canonical Allele Identifier: CA12466134
Gene: SUN3 HGNC NCBI

Linked Data

dbSNP Id: rs10951937
gnomAD v2: 7-48031624-A-C
gnomAD v3: 7-47992027-A-C
gnomAD v4: 7-47992027-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.47992027A>C , CM000669.2:g.47992027A>C GRCh38
NC_000007.13:g.48031624A>C , CM000669.1:g.48031624A>C GRCh37
NC_000007.12:g.47998149A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297325.9:c.861+2288T>G MANE Select ENSP00000297325.4:n.861+2288T>G
ENST00000297325.8:c.861+2288T>G ENSP00000297325.4:n.861+2288T>G
ENST00000395572.6:c.861+2288T>G ENSP00000378939.2:n.861+2288T>G
ENST00000412142.5:c.825+2288T>G ENSP00000410204.2:n.825+2288T>G
ENST00000412371.5:c.327+2288T>G ENSP00000406887.1:n.327+2288T>G
ENST00000438771.5:c.562-982T>G ENSP00000409077.1:n.562-982T>G
ENST00000449896.2:c.*689+2288T>G ENSP00000395392.2:n.*689+2288T>G
ENST00000453071.5:c.632+2288T>G
ENST00000453192.3:c.573+2276T>G ENSP00000387525.3:n.573+2276T>G
ENST00000473723.5:n.339-982T>G
NM_001030019.1:c.861+2288T>G NP_001025190.1:n.861+2288T>G
NM_001284350.1:c.825+2288T>G NP_001271279.1:n.825+2288T>G
NM_152782.3:c.861+2288T>G NP_689995.3:n.861+2288T>G
XM_011515252.1:c.883-982T>G XP_011513554.1:n.883-982T>G
XM_011515253.1:c.583-982T>G XP_011513555.1:n.583-982T>G
XM_017011930.1:c.861+2288T>G XP_016867419.1:n.861+2288T>G
XR_002956417.1:n.1148+864T>G
NM_001030019.2:c.861+2288T>G MANE Select NP_001025190.1:n.861+2288T>G
NM_001284350.2:c.825+2288T>G NP_001271279.1:n.825+2288T>G
NM_152782.4:c.861+2288T>G NP_689995.3:n.861+2288T>G