Canonical Allele Identifier: CA3613870

Gene: EXOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.629868C>T , CM000668.2:g.629868C>T	GRCh38
NC_000006.11:g.629868C>T , CM000668.1:g.629868C>T	GRCh37
NC_000006.10:g.574868C>T	NCBI36
NG_047166.1:g.68274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230449.9:c.389G>A MANE Select	ENSP00000230449.4:p.Arg130His
ENST00000230449.8:c.389G>A	ENSP00000230449.4:p.Arg130His
ENST00000443083.5:c.389G>A	ENSP00000406400.1:p.Arg130His
NM_018303.5:c.389G>A	NP_060773.3:p.Arg130His
NR_073064.1:n.717G>A
XM_017011018.1:c.389G>A	XP_016866507.1:p.Arg130His
XM_017011019.1:c.389G>A	XP_016866508.1:p.Arg130His
XM_017011020.1:c.389G>A	XP_016866509.1:p.Arg130His
XM_017011021.1:c.389G>A	XP_016866510.1:p.Arg130His
XM_017011022.1:c.389G>A	XP_016866511.1:p.Arg130His
XM_017011023.1:c.389G>A	XP_016866512.1:p.Arg130His
XM_017011024.1:c.389G>A	XP_016866513.1:p.Arg130His
XM_017011025.1:c.389G>A	XP_016866514.1:p.Arg130His
XM_017011026.1:c.389G>A	XP_016866515.1:p.Arg130His
NM_018303.6:c.389G>A MANE Select	NP_060773.3:p.Arg130His
NR_073064.2:n.715G>A