Canonical Allele Identifier: CA2837684769

Gene: EXOC1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55885609dup , CM000666.2:g.55885609dup	GRCh38
NC_000004.11:g.56751775dup , CM000666.1:g.56751775dup	GRCh37
NC_000004.10:g.56446532dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381295.7:c.1330+1681dup MANE Select	ENSP00000370695.2:n.1330+1681dup
ENST00000346134.11:c.1330+1681dup	ENSP00000326514.7:n.1330+1681dup
ENST00000349598.6:c.1330+1681dup	ENSP00000334431.6:n.1330+1681dup
ENST00000381295.6:c.1330+1681dup	ENSP00000370695.2:n.1330+1681dup
ENST00000509302.5:n.161+1681dup
ENST00000511971.5:n.1202+1681dup
NM_001024924.1:c.1330+1681dup	NP_001020095.1:n.1330+1681dup
NM_018261.3:c.1330+1681dup	NP_060731.2:n.1330+1681dup
NM_178237.2:c.1330+1681dup	NP_839955.1:n.1330+1681dup
XM_005265747.1:c.1384+1681dup	XP_005265804.1:n.1384+1681dup
XM_005265748.1:c.1384+1681dup	XP_005265805.1:n.1384+1681dup
XM_005265750.1:c.1330+1681dup	XP_005265807.1:n.1330+1681dup
XM_011534388.1:c.1405+1681dup	XP_011532690.1:n.1405+1681dup
XM_011534389.1:c.1405+1681dup	XP_011532691.1:n.1405+1681dup
XM_011534390.1:c.1405+1681dup	XP_011532692.1:n.1405+1681dup
XM_011534391.1:c.1351+1681dup	XP_011532693.1:n.1351+1681dup
XM_011534392.1:c.1351+1681dup	XP_011532694.1:n.1351+1681dup
XM_011534393.1:c.1405+1681dup	XP_011532695.1:n.1405+1681dup
XM_005265747.3:c.1384+1681dup	XP_005265804.1:n.1384+1681dup
XM_005265750.3:c.1330+1681dup	XP_005265807.1:n.1330+1681dup
XM_017008405.2:c.1384+1681dup	XP_016863894.1:n.1384+1681dup
XM_017008406.1:c.1384+1681dup	XP_016863895.1:n.1384+1681dup
XM_017008407.2:c.1384+1681dup	XP_016863896.1:n.1384+1681dup
XM_017008408.2:c.157+1681dup	XP_016863897.1:n.157+1681dup
XM_017008409.1:c.157+1681dup	XP_016863898.1:n.157+1681dup
XR_001741285.2:n.1689+1681dup
XR_001741286.1:n.1490+1681dup
NM_001024924.2:c.1330+1681dup MANE Select	NP_001020095.1:n.1330+1681dup
NM_018261.4:c.1330+1681dup	NP_060731.2:n.1330+1681dup
NM_178237.3:c.1330+1681dup	NP_839955.1:n.1330+1681dup