Canonical Allele Identifier: CA2546854172
Gene: EXOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.577826_577827insAGGTAGATAAGAGGAAGAGGTGAC , CM000668.2:g.577826_577827insAGGTAGATAAGAGGAAGAGGTGAC GRCh38
NC_000006.11:g.577826_577827insAGGTAGATAAGAGGAAGAGGTGAC , CM000668.1:g.577826_577827insAGGTAGATAAGAGGAAGAGGTGAC GRCh37
NC_000006.10:g.522826_522827insAGGTAGATAAGAGGAAGAGGTGAC NCBI36
NG_047166.1:g.120315_120316insGTCACCTCTTCCTCTTATCTACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000230449.9:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT MANE Select ENSP00000230449.4:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTA...
ENST00000230449.8:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT ENSP00000230449.4:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTA...
NM_018303.5:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT NP_060773.3:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT
NR_073064.1:n.1521-945_1521-944insGTCACCTCTTCCTCTTATCTACCT
XM_017011018.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866507.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011019.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866508.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011020.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866509.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011021.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866510.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011022.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866511.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011023.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866512.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011024.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866513.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011025.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866514.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
XM_017011026.1:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT XP_016866515.1:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT...
NM_018303.6:c.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT MANE Select NP_060773.3:n.1193-945_1193-944insGTCACCTCTTCCTCTTATCTACCT
NR_073064.2:n.1519-945_1519-944insGTCACCTCTTCCTCTTATCTACCT