Canonical Allele Identifier: CA409312974

Gene: ARFGEF2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.48998233G>A , CM000682.2:g.48998233G>A	GRCh38
NC_000020.10:g.47614770G>A , CM000682.1:g.47614770G>A	GRCh37
NC_000020.9:g.47048177G>A	NCBI36
NG_011490.1:g.81496G>A
NG_011490.2:g.81496G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006420.3:c.3262G>A MANE Select	NP_006411.2:p.Val1088Ile
ENST00000371917.5:c.3262G>A MANE Select	ENSP00000360985.4:p.Val1088Ile
NM_006420.2:c.3262G>A	NP_006411.2:p.Val1088Ile
ENST00000371917.4:c.3262G>A	ENSP00000360985.4:p.Val1088Ile
ENST00000493140.1:n.134G>A
ENST00000679436.1:c.3259G>A	ENSP00000504888.1:p.Val1087Ile
ENST00000679542.1:n.2819G>A
ENST00000680635.1:n.2819G>A
ENST00000680871.1:c.3110G>A	ENSP00000505042.1:n.3110G>A
ENST00000681021.1:c.3262G>A	ENSP00000505972.1:p.Val1088Ile
ENST00000681399.1:c.*2939G>A	ENSP00000506363.1:n.*2939G>A
ENST00000681656.1:c.3153G>A	ENSP00000505638.1:n.3153G>A
ENST00000681885.1:c.3262G>A	ENSP00000505737.1:p.Val1088Ile
XM_005260252.2:c.3259G>A	XP_005260309.1:p.Val1087Ile
XM_005260252.3:c.3259G>A	XP_005260309.1:p.Val1087Ile