Canonical Allele Identifier: CA1459296143
Gene: EXOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55885496_55885497delinsGT , CM000666.2:g.55885496_55885497delinsGT GRCh38
NC_000004.11:g.56751662_56751663delinsGT , CM000666.1:g.56751662_56751663delinsGT GRCh37
NC_000004.10:g.56446419_56446420delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381295.7:c.1330+1568_1330+1569delinsGT MANE Select ENSP00000370695.2:n.1330+1568_1330+1569de...
ENST00000346134.11:c.1330+1568_1330+1569delinsGT ENSP00000326514.7:n.1330+1568_1330+1569de...
ENST00000349598.6:c.1330+1568_1330+1569delinsGT ENSP00000334431.6:n.1330+1568_1330+1569de...
ENST00000381295.6:c.1330+1568_1330+1569delinsGT ENSP00000370695.2:n.1330+1568_1330+1569de...
ENST00000509302.5:n.161+1568_161+1569delinsGT
ENST00000511971.5:n.1202+1568_1202+1569delinsGT
NM_001024924.1:c.1330+1568_1330+1569delinsGT NP_001020095.1:n.1330+1568_1330+1569delin...
NM_018261.3:c.1330+1568_1330+1569delinsGT NP_060731.2:n.1330+1568_1330+1569delinsGT...
NM_178237.2:c.1330+1568_1330+1569delinsGT NP_839955.1:n.1330+1568_1330+1569delinsGT...
XM_005265747.1:c.1384+1568_1384+1569delinsGT XP_005265804.1:n.1384+1568_1384+1569delin...
XM_005265748.1:c.1384+1568_1384+1569delinsGT XP_005265805.1:n.1384+1568_1384+1569delin...
XM_005265750.1:c.1330+1568_1330+1569delinsGT XP_005265807.1:n.1330+1568_1330+1569delin...
XM_011534388.1:c.1405+1568_1405+1569delinsGT XP_011532690.1:n.1405+1568_1405+1569delin...
XM_011534389.1:c.1405+1568_1405+1569delinsGT XP_011532691.1:n.1405+1568_1405+1569delin...
XM_011534390.1:c.1405+1568_1405+1569delinsGT XP_011532692.1:n.1405+1568_1405+1569delin...
XM_011534391.1:c.1351+1568_1351+1569delinsGT XP_011532693.1:n.1351+1568_1351+1569delin...
XM_011534392.1:c.1351+1568_1351+1569delinsGT XP_011532694.1:n.1351+1568_1351+1569delin...
XM_011534393.1:c.1405+1568_1405+1569delinsGT XP_011532695.1:n.1405+1568_1405+1569delin...
XM_005265747.3:c.1384+1568_1384+1569delinsGT XP_005265804.1:n.1384+1568_1384+1569delin...
XM_005265750.3:c.1330+1568_1330+1569delinsGT XP_005265807.1:n.1330+1568_1330+1569delin...
XM_017008405.2:c.1384+1568_1384+1569delinsGT XP_016863894.1:n.1384+1568_1384+1569delin...
XM_017008406.1:c.1384+1568_1384+1569delinsGT XP_016863895.1:n.1384+1568_1384+1569delin...
XM_017008407.2:c.1384+1568_1384+1569delinsGT XP_016863896.1:n.1384+1568_1384+1569delin...
XM_017008408.2:c.157+1568_157+1569delinsGT XP_016863897.1:n.157+1568_157+1569delinsG...
XM_017008409.1:c.157+1568_157+1569delinsGT XP_016863898.1:n.157+1568_157+1569delinsG...
XR_001741285.2:n.1689+1568_1689+1569delinsGT
XR_001741286.1:n.1490+1568_1490+1569delinsGT
NM_001024924.2:c.1330+1568_1330+1569delinsGT MANE Select NP_001020095.1:n.1330+1568_1330+1569delin...
NM_018261.4:c.1330+1568_1330+1569delinsGT NP_060731.2:n.1330+1568_1330+1569delinsGT...
NM_178237.3:c.1330+1568_1330+1569delinsGT NP_839955.1:n.1330+1568_1330+1569delinsGT...