Canonical Allele Identifier: CA2619487209

Gene: ARHGEF25

Linked Data

• gnomAD v4: 12-57614295-GTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57614297_57614299del , CM000674.2:g.57614297_57614299del	GRCh38
NC_000012.11:g.58008080_58008082del , CM000674.1:g.58008080_58008082del	GRCh37
NC_000012.10:g.56294347_56294349del	NCBI36
NG_053182.1:g.9118_9120del
NG_053182.2:g.9182_9184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286494.9:c.657-34_657-32del MANE Select	ENSP00000286494.4:n.657-34_657-32del
ENST00000286494.8:c.657-34_657-32del	ENSP00000286494.4:n.657-34_657-32del
ENST00000333972.11:c.774-34_774-32del	ENSP00000335560.7:n.774-34_774-32del
ENST00000471370.5:n.304_306del
ENST00000616622.1:c.339-34_339-32del	ENSP00000484303.1:n.339-34_339-32del
NM_001111270.2:c.774-34_774-32del	NP_001104740.1:n.774-34_774-32del
NM_182947.3:c.657-34_657-32del	NP_891992.2:n.657-34_657-32del
NR_046223.1:n.1147-34_1147-32del
NM_001347933.1:c.657-34_657-32del	NP_001334862.1:n.657-34_657-32del
NM_182947.4:c.657-34_657-32del MANE Select	NP_891992.3:n.657-34_657-32del
NM_001111270.3:c.774-34_774-32del	NP_001104740.2:n.774-34_774-32del
NM_001347933.2:c.657-34_657-32del	NP_001334862.2:n.657-34_657-32del
NR_046223.2:n.1147-34_1147-32del