Canonical Allele Identifier: CA14799618

Gene: ARFGEF2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.48925063G>A , CM000682.2:g.48925063G>A	GRCh38
NC_000020.10:g.47541600G>A , CM000682.1:g.47541600G>A	GRCh37
NC_000020.9:g.46975007G>A	NCBI36
NG_011490.1:g.8326G>A
NG_011490.2:g.8326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371917.5:c.121+3053G>A MANE Select	ENSP00000360985.4:n.121+3053G>A
ENST00000679436.1:c.121+3053G>A	ENSP00000504888.1:n.121+3053G>A
ENST00000680871.1:c.121+3053G>A	ENSP00000505042.1:n.121+3053G>A
ENST00000681021.1:c.121+3053G>A	ENSP00000505972.1:n.121+3053G>A
ENST00000681399.1:c.121+3053G>A	ENSP00000506363.1:n.121+3053G>A
ENST00000681656.1:c.121+3053G>A	ENSP00000505638.1:n.121+3053G>A
ENST00000681885.1:c.121+3053G>A	ENSP00000505737.1:n.121+3053G>A
ENST00000371917.4:c.121+3053G>A	ENSP00000360985.4:n.121+3053G>A
NM_006420.2:c.121+3053G>A	NP_006411.2:n.121+3053G>A
XM_005260252.2:c.121+3053G>A	XP_005260309.1:n.121+3053G>A
XM_005260252.3:c.121+3053G>A	XP_005260309.1:n.121+3053G>A
NM_006420.3:c.121+3053G>A MANE Select	NP_006411.2:n.121+3053G>A