Canonical Allele Identifier: CA174900

Gene: ARHGEF25

Linked Data

• ClinVar Variation Id: 161847
• ClinVar RCV Id: RCV000149383
• dbSNP Id: rs193921117
• COSMIC: COSM5521466 ; COSM5521467
• MyVariant Identifiers: chr12:g.58008107C>A (hg19) ; chr12:g.57614324C>A (hg38)
• PubMed: PMID:23265383

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614324C>A , CM000674.2:g.57614324C>A	GRCh38
NC_000012.11:g.58008107C>A , CM000674.1:g.58008107C>A	GRCh37
NC_000012.10:g.56294374C>A	NCBI36
NG_053182.1:g.9145C>A
NG_053182.2:g.9209C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000286494.9:c.657-7C>A MANE Select	ENSP00000286494.4:n.657-7C>A
ENST00000286494.8:c.657-7C>A	ENSP00000286494.4:n.657-7C>A
ENST00000333972.11:c.774-7C>A	ENSP00000335560.7:n.774-7C>A
ENST00000471370.5:n.331C>A
ENST00000616622.1:c.339-7C>A	ENSP00000484303.1:n.339-7C>A
NM_001111270.2:c.774-7C>A	NP_001104740.1:n.774-7C>A
NM_182947.3:c.657-7C>A	NP_891992.2:n.657-7C>A
NR_046223.1:n.1147-7C>A
NM_001347933.1:c.657-7C>A	NP_001334862.1:n.657-7C>A
NM_182947.4:c.657-7C>A MANE Select	NP_891992.3:n.657-7C>A
NM_001111270.3:c.774-7C>A	NP_001104740.2:n.774-7C>A
NM_001347933.2:c.657-7C>A	NP_001334862.2:n.657-7C>A
NR_046223.2:n.1147-7C>A