Canonical Allele Identifier: CA753549545

Gene: ARHGAP8 PRR5-ARHGAP8

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.44754779C>G , CM000684.2:g.44754779C>G	GRCh38
NC_000022.10:g.45150659C>G , CM000684.1:g.45150659C>G	GRCh37
NC_000022.9:g.43529323C>G	NCBI36
NG_046967.1:g.57582C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356099.11:c.-72+2152C>G (ARHGAP8) MANE Select	ENSP00000348407.6:n.-72+2152C>G
ENST00000336963.8:c.-72+2152C>G (ARHGAP8)	ENSP00000337287.4:n.-72+2152C>G
ENST00000352766.11:c.691+19617C>G (PRR5-ARHGAP8)	ENSP00000262731.11:n.691+19617C>G
ENST00000356099.10:c.-72+2152C>G (ARHGAP8)	ENSP00000348407.6:n.-72+2152C>G
ENST00000361473.9:c.322+28145C>G (PRR5-ARHGAP8)	ENSP00000354732.5:n.322+28145C>G
ENST00000389774.6:c.-72+2152C>G (ARHGAP8)	ENSP00000374424.2:n.-72+2152C>G
ENST00000396119.6:c.-140+2152C>G (ARHGAP8)	ENSP00000379425.2:n.-140+2152C>G
ENST00000412433.5:c.-200+2039C>G (ARHGAP8)	ENSP00000402775.1:n.-200+2039C>G
ENST00000447333.5:c.-72+2152C>G (ARHGAP8)	ENSP00000403618.1:n.-72+2152C>G
ENST00000460809.5:n.54+2152C>G (ARHGAP8)
ENST00000495250.2:n.105+28145C>G (PRR5-ARHGAP8)
ENST00000515632.2:c.90+28145C>G (PRR5-ARHGAP8)
NM_001017526.1:c.-72+2152C>G (ARHGAP8)	NP_001017526.1:n.-72+2152C>G
NM_001198726.1:c.-72+2152C>G (ARHGAP8)	NP_001185655.1:n.-72+2152C>G
NM_181334.5:c.322+28145C>G (PRR5-ARHGAP8)	NP_851851.3:n.322+28145C>G
NM_181335.2:c.-72+2152C>G (ARHGAP8)	NP_851852.2:n.-72+2152C>G
NM_001017526.2:c.-72+2152C>G (ARHGAP8)	NP_001017526.1:n.-72+2152C>G
NM_001198726.2:c.-72+2152C>G (ARHGAP8)	NP_001185655.1:n.-72+2152C>G
NM_181334.6:c.322+28145C>G (PRR5-ARHGAP8)	NP_851851.3:n.322+28145C>G
NM_181335.3:c.-72+2152C>G (ARHGAP8) MANE Select	NP_851852.2:n.-72+2152C>G