Canonical Allele Identifier: CA1098031636

Gene: RAC1

Linked Data

• gnomAD v3: 7-6391813-C-CG
• gnomAD v4: 7-6391813-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391813_6391814insG , CM000669.2:g.6391813_6391814insG	GRCh38
NC_000007.13:g.6431444_6431445insG , CM000669.1:g.6431444_6431445insG	GRCh37
NC_000007.12:g.6397969_6397970insG	NCBI36
NG_029431.1:g.22319_22320insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.296-111_296-110insG
ENST00000704002.1:c.207-111_207-110insG	ENSP00000515615.1:n.207-111_207-110insG
ENST00000704003.1:c.*61-111_*61-110insG	ENSP00000515616.1:n.*61-111_*61-110insG
ENST00000348035.9:c.108-111_108-110insG MANE Select	ENSP00000258737.7:n.108-111_108-110insG
ENST00000348035.8:c.108-111_108-110insG	ENSP00000258737.7:n.108-111_108-110insG
ENST00000356142.4:c.108-111_108-110insG	ENSP00000348461.4:n.108-111_108-110insG
ENST00000488373.5:n.339-111_339-110insG
ENST00000497741.5:n.124-111_124-110insG
NM_006908.4:c.108-111_108-110insG	NP_008839.2:n.108-111_108-110insG
NM_018890.3:c.108-111_108-110insG	NP_061485.1:n.108-111_108-110insG
NM_006908.5:c.108-111_108-110insG MANE Select	NP_008839.2:n.108-111_108-110insG
NM_018890.4:c.108-111_108-110insG	NP_061485.1:n.108-111_108-110insG