Canonical Allele Identifier: CA2543989570

Gene: EXOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.577814_577815insAG , CM000668.2:g.577814_577815insAG	GRCh38
NC_000006.11:g.577814_577815insAG , CM000668.1:g.577814_577815insAG	GRCh37
NC_000006.10:g.522814_522815insAG	NCBI36
NG_047166.1:g.120327_120328insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000230449.9:c.1193-933_1193-932insCT MANE Select	ENSP00000230449.4:n.1193-933_1193-932insCT
ENST00000230449.8:c.1193-933_1193-932insCT	ENSP00000230449.4:n.1193-933_1193-932insCT
NM_018303.5:c.1193-933_1193-932insCT	NP_060773.3:n.1193-933_1193-932insCT
NR_073064.1:n.1521-933_1521-932insCT
XM_017011018.1:c.1193-933_1193-932insCT	XP_016866507.1:n.1193-933_1193-932insCT
XM_017011019.1:c.1193-933_1193-932insCT	XP_016866508.1:n.1193-933_1193-932insCT
XM_017011020.1:c.1193-933_1193-932insCT	XP_016866509.1:n.1193-933_1193-932insCT
XM_017011021.1:c.1193-933_1193-932insCT	XP_016866510.1:n.1193-933_1193-932insCT
XM_017011022.1:c.1193-933_1193-932insCT	XP_016866511.1:n.1193-933_1193-932insCT
XM_017011023.1:c.1193-933_1193-932insCT	XP_016866512.1:n.1193-933_1193-932insCT
XM_017011024.1:c.1193-933_1193-932insCT	XP_016866513.1:n.1193-933_1193-932insCT
XM_017011025.1:c.1193-933_1193-932insCT	XP_016866514.1:n.1193-933_1193-932insCT
XM_017011026.1:c.1193-933_1193-932insCT	XP_016866515.1:n.1193-933_1193-932insCT
NM_018303.6:c.1193-933_1193-932insCT MANE Select	NP_060773.3:n.1193-933_1193-932insCT
NR_073064.2:n.1519-933_1519-932insCT