Canonical Allele Identifier: CA2511644974
Gene: EXOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.577805_577806insATGTCAGAGGGCA , CM000668.2:g.577805_577806insATGTCAGAGGGCA GRCh38
NC_000006.11:g.577805_577806insATGTCAGAGGGCA , CM000668.1:g.577805_577806insATGTCAGAGGGCA GRCh37
NC_000006.10:g.522805_522806insATGTCAGAGGGCA NCBI36
NG_047166.1:g.120336_120337insTGCCCTCTGACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000230449.9:c.1193-924_1193-923insTGCCCTCTGACAT MANE Select ENSP00000230449.4:n.1193-924_1193-923insTGCCCTCTGACAT
ENST00000230449.8:c.1193-924_1193-923insTGCCCTCTGACAT ENSP00000230449.4:n.1193-924_1193-923insTGCCCTCTGACAT
NM_018303.5:c.1193-924_1193-923insTGCCCTCTGACAT NP_060773.3:n.1193-924_1193-923insTGCCCTCTGACAT
NR_073064.1:n.1521-924_1521-923insTGCCCTCTGACAT
XM_017011018.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866507.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011019.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866508.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011020.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866509.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011021.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866510.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011022.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866511.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011023.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866512.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011024.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866513.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011025.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866514.1:n.1193-924_1193-923insTGCCCTCTGACAT
XM_017011026.1:c.1193-924_1193-923insTGCCCTCTGACAT XP_016866515.1:n.1193-924_1193-923insTGCCCTCTGACAT
NM_018303.6:c.1193-924_1193-923insTGCCCTCTGACAT MANE Select NP_060773.3:n.1193-924_1193-923insTGCCCTCTGACAT
NR_073064.2:n.1519-924_1519-923insTGCCCTCTGACAT