Canonical Allele Identifier: CA1705426290
Gene: SUN3 HGNC NCBI

Linked Data

dbSNP Id: rs1789073700

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.47991852_47991853insCAGAGAAA , CM000669.2:g.47991852_47991853insCAGAGAAA GRCh38
NC_000007.13:g.48031449_48031450insCAGAGAAA , CM000669.1:g.48031449_48031450insCAGAGAAA GRCh37
NC_000007.12:g.47997974_47997975insCAGAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297325.9:c.861+2462_861+2463insTTTCTCTG MANE Select ENSP00000297325.4:n.861+2462_861+2463insTTTCTCTG
ENST00000297325.8:c.861+2462_861+2463insTTTCTCTG ENSP00000297325.4:n.861+2462_861+2463insTTTCTCTG
ENST00000395572.6:c.861+2462_861+2463insTTTCTCTG ENSP00000378939.2:n.861+2462_861+2463insTTTCTCTG
ENST00000412142.5:c.825+2462_825+2463insTTTCTCTG ENSP00000410204.2:n.825+2462_825+2463insTTTCTCTG
ENST00000412371.5:c.327+2462_327+2463insTTTCTCTG ENSP00000406887.1:n.327+2462_327+2463insTTTCTCTG
ENST00000438771.5:c.562-808_562-807insTTTCTCTG ENSP00000409077.1:n.562-808_562-807insTTTCTCTG
ENST00000449896.2:c.*689+2462_*689+2463insTTTCTCTG ENSP00000395392.2:n.*689+2462_*689+2463insTTTCTCTG
ENST00000453071.5:c.632+2462_632+2463insTTTCTCTG
ENST00000453192.3:c.573+2450_573+2451insTTTCTCTG ENSP00000387525.3:n.573+2450_573+2451insTTTCTCTG
ENST00000473723.5:n.339-808_339-807insTTTCTCTG
NM_001030019.1:c.861+2462_861+2463insTTTCTCTG NP_001025190.1:n.861+2462_861+2463insTTTCTCTG
NM_001284350.1:c.825+2462_825+2463insTTTCTCTG NP_001271279.1:n.825+2462_825+2463insTTTCTCTG
NM_152782.3:c.861+2462_861+2463insTTTCTCTG NP_689995.3:n.861+2462_861+2463insTTTCTCTG
XM_011515252.1:c.883-808_883-807insTTTCTCTG XP_011513554.1:n.883-808_883-807insTTTCTCTG
XM_011515253.1:c.583-808_583-807insTTTCTCTG XP_011513555.1:n.583-808_583-807insTTTCTCTG
XM_017011930.1:c.861+2462_861+2463insTTTCTCTG XP_016867419.1:n.861+2462_861+2463insTTTCTCTG
XR_002956417.1:n.1148+1038_1148+1039insTTTCTCTG
NM_001030019.2:c.861+2462_861+2463insTTTCTCTG MANE Select NP_001025190.1:n.861+2462_861+2463insTTTCTCTG
NM_001284350.2:c.825+2462_825+2463insTTTCTCTG NP_001271279.1:n.825+2462_825+2463insTTTCTCTG
NM_152782.4:c.861+2462_861+2463insTTTCTCTG NP_689995.3:n.861+2462_861+2463insTTTCTCTG