Canonical Allele Identifier: CA2681706097

Gene: RAC1

Linked Data

• gnomAD v4: 7-6392077-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392077_6392078insC , CM000669.2:g.6392077_6392078insC	GRCh38
NC_000007.13:g.6431708_6431709insC , CM000669.1:g.6431708_6431709insC	GRCh37
NC_000007.12:g.6398233_6398234insC	NCBI36
NG_029431.1:g.22583_22584insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.449_450insC
ENST00000704002.1:c.324+36_324+37insC	ENSP00000515615.1:n.324+36_324+37insC
ENST00000704003.1:c.*178+36_*178+37insC	ENSP00000515616.1:n.*178+36_*178+37insC
ENST00000348035.9:c.225+36_225+37insC MANE Select	ENSP00000258737.7:n.225+36_225+37insC
ENST00000348035.8:c.225+36_225+37insC	ENSP00000258737.7:n.225+36_225+37insC
ENST00000356142.4:c.225+36_225+37insC	ENSP00000348461.4:n.225+36_225+37insC
ENST00000488373.5:n.456+36_456+37insC
ENST00000497741.5:n.241+36_241+37insC
NM_006908.4:c.225+36_225+37insC	NP_008839.2:n.225+36_225+37insC
NM_018890.3:c.225+36_225+37insC	NP_061485.1:n.225+36_225+37insC
NM_006908.5:c.225+36_225+37insC MANE Select	NP_008839.2:n.225+36_225+37insC
NM_018890.4:c.225+36_225+37insC	NP_061485.1:n.225+36_225+37insC