Canonical Allele Identifier: CA1605317003

Gene: EXOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.542159A= , CM000668.2:g.542159A=	GRCh38
NC_000006.11:g.542159A= , CM000668.1:g.542159A=	GRCh37
NC_000006.10:g.487159A=	NCBI36
NG_047166.1:g.155983T=

Transcript Alleles

HGVS	Amino-acid Change
NM_018303.6:c.2238+7016T= MANE Select	NP_060773.3:n.2238+7016T=
ENST00000230449.9:c.2238+7016T= MANE Select	ENSP00000230449.4:n.2238+7016T=
NM_018303.5:c.2238+7016T=	NP_060773.3:n.2238+7016T=
NR_073064.1:n.2566+7016T=
NR_073064.2:n.2564+7016T=
ENST00000230449.8:c.2238+7016T=	ENSP00000230449.4:n.2238+7016T=
XM_017011018.1:c.2238+7016T=	XP_016866507.1:n.2238+7016T=
XM_017011019.1:c.2238+7016T=	XP_016866508.1:n.2238+7016T=
XM_017011020.1:c.2238+7016T=	XP_016866509.1:n.2238+7016T=
XM_017011021.1:c.2238+7016T=	XP_016866510.1:n.2238+7016T=
XM_017011022.1:c.2238+7016T=	XP_016866511.1:n.2238+7016T=
XM_017011023.1:c.2238+7016T=	XP_016866512.1:n.2238+7016T=
XM_017011024.1:c.2238+7016T=	XP_016866513.1:n.2238+7016T=
XM_017011025.1:c.2238+7016T=	XP_016866514.1:n.2238+7016T=
XM_017011026.1:c.2238+7016T=	XP_016866515.1:n.2238+7016T=