Canonical Allele Identifier: CA2038946502

Gene: ARHGEF25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614321_57614323delinsACC , CM000674.2:g.57614321_57614323delinsACC	GRCh38
NC_000012.11:g.58008104_58008106delinsACC , CM000674.1:g.58008104_58008106delinsACC	GRCh37
NC_000012.10:g.56294371_56294373delinsACC	NCBI36
NG_053182.1:g.9142_9144delinsACC
NG_053182.2:g.9206_9208delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286494.9:c.657-10_657-8delinsACC MANE Select	ENSP00000286494.4:n.657-10_657-8delinsACC
ENST00000286494.8:c.657-10_657-8delinsACC	ENSP00000286494.4:n.657-10_657-8delinsACC
ENST00000333972.11:c.774-10_774-8delinsACC	ENSP00000335560.7:n.774-10_774-8delinsACC
ENST00000471370.5:n.328_330delinsACC
ENST00000616622.1:c.339-10_339-8delinsACC	ENSP00000484303.1:n.339-10_339-8delinsACC
NM_001111270.2:c.774-10_774-8delinsACC	NP_001104740.1:n.774-10_774-8delinsACC
NM_182947.3:c.657-10_657-8delinsACC	NP_891992.2:n.657-10_657-8delinsACC
NR_046223.1:n.1147-10_1147-8delinsACC
NM_001347933.1:c.657-10_657-8delinsACC	NP_001334862.1:n.657-10_657-8delinsACC
NM_182947.4:c.657-10_657-8delinsACC MANE Select	NP_891992.3:n.657-10_657-8delinsACC
NM_001111270.3:c.774-10_774-8delinsACC	NP_001104740.2:n.774-10_774-8delinsACC
NM_001347933.2:c.657-10_657-8delinsACC	NP_001334862.2:n.657-10_657-8delinsACC
NR_046223.2:n.1147-10_1147-8delinsACC