Canonical Allele Identifier: CA605705969

Gene: ARHGEF25

Linked Data

• dbSNP Id: rs1312113390
• gnomAD v2: 12-58008066-G-A
• MyVariant Identifiers: chr12:g.58008066G>A (hg19) ; chr12:g.57614283G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614283G>A , CM000674.2:g.57614283G>A	GRCh38
NC_000012.11:g.58008066G>A , CM000674.1:g.58008066G>A	GRCh37
NC_000012.10:g.56294333G>A	NCBI36
NG_053182.1:g.9104G>A
NG_053182.2:g.9168G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286494.9:c.657-48G>A MANE Select	ENSP00000286494.4:n.657-48G>A
ENST00000286494.8:c.657-48G>A	ENSP00000286494.4:n.657-48G>A
ENST00000333972.11:c.774-48G>A	ENSP00000335560.7:n.774-48G>A
ENST00000471370.5:n.290G>A
ENST00000616622.1:c.339-48G>A	ENSP00000484303.1:n.339-48G>A
NM_001111270.2:c.774-48G>A	NP_001104740.1:n.774-48G>A
NM_182947.3:c.657-48G>A	NP_891992.2:n.657-48G>A
NR_046223.1:n.1147-48G>A
NM_001347933.1:c.657-48G>A	NP_001334862.1:n.657-48G>A
NM_182947.4:c.657-48G>A MANE Select	NP_891992.3:n.657-48G>A
NM_001111270.3:c.774-48G>A	NP_001104740.2:n.774-48G>A
NM_001347933.2:c.657-48G>A	NP_001334862.2:n.657-48G>A
NR_046223.2:n.1147-48G>A