Canonical Allele Identifier: CA2038946470

Gene: ARHGEF25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614294T= , CM000674.2:g.57614294T=	GRCh38
NC_000012.11:g.58008077T= , CM000674.1:g.58008077T=	GRCh37
NC_000012.10:g.56294344T=	NCBI36
NG_053182.1:g.9115T=
NG_053182.2:g.9179T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286494.9:c.657-37T= MANE Select	ENSP00000286494.4:n.657-37T=
ENST00000286494.8:c.657-37T=	ENSP00000286494.4:n.657-37T=
ENST00000333972.11:c.774-37T=	ENSP00000335560.7:n.774-37T=
ENST00000471370.5:n.301T=
ENST00000616622.1:c.339-37T=	ENSP00000484303.1:n.339-37T=
NM_001111270.2:c.774-37T=	NP_001104740.1:n.774-37T=
NM_182947.3:c.657-37T=	NP_891992.2:n.657-37T=
NR_046223.1:n.1147-37T=
NM_001347933.1:c.657-37T=	NP_001334862.1:n.657-37T=
NM_182947.4:c.657-37T= MANE Select	NP_891992.3:n.657-37T=
NM_001111270.3:c.774-37T=	NP_001104740.2:n.774-37T=
NM_001347933.2:c.657-37T=	NP_001334862.2:n.657-37T=
NR_046223.2:n.1147-37T=