Canonical Allele Identifier: CA2581535237

Gene: EXOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.566741A>T , CM000668.2:g.566741A>T	GRCh38
NC_000006.11:g.566741A>T , CM000668.1:g.566741A>T	GRCh37
NC_000006.10:g.511741A>T	NCBI36
NG_047166.1:g.131401T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018303.6:c.1444-1812T>A MANE Select	NP_060773.3:n.1444-1812T>A
ENST00000230449.9:c.1444-1812T>A MANE Select	ENSP00000230449.4:n.1444-1812T>A
NM_018303.5:c.1444-1812T>A	NP_060773.3:n.1444-1812T>A
NR_073064.1:n.1772-1812T>A
NR_073064.2:n.1770-1812T>A
ENST00000230449.8:c.1444-1812T>A	ENSP00000230449.4:n.1444-1812T>A
XM_017011018.1:c.1444-1812T>A	XP_016866507.1:n.1444-1812T>A
XM_017011019.1:c.1444-1812T>A	XP_016866508.1:n.1444-1812T>A
XM_017011020.1:c.1444-1812T>A	XP_016866509.1:n.1444-1812T>A
XM_017011021.1:c.1444-1812T>A	XP_016866510.1:n.1444-1812T>A
XM_017011022.1:c.1444-1812T>A	XP_016866511.1:n.1444-1812T>A
XM_017011023.1:c.1444-1812T>A	XP_016866512.1:n.1444-1812T>A
XM_017011024.1:c.1444-1812T>A	XP_016866513.1:n.1444-1812T>A
XM_017011025.1:c.1444-1812T>A	XP_016866514.1:n.1444-1812T>A
XM_017011026.1:c.1444-1812T>A	XP_016866515.1:n.1444-1812T>A