Canonical Allele Identifier: CA1685476982

Gene: RAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6392290_6392291delinsCG , CM000669.2:g.6392290_6392291delinsCG	GRCh38
NC_000007.13:g.6431921_6431922delinsCG , CM000669.1:g.6431921_6431922delinsCG	GRCh37
NC_000007.12:g.6398446_6398447delinsCG	NCBI36
NG_029431.1:g.22796_22797delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.662_663delinsCG
ENST00000704002.1:c.324+249_324+250delinsCG	ENSP00000515615.1:n.324+249_324+250delinsCG
ENST00000704003.1:c.*178+249_*178+250delinsCG	ENSP00000515616.1:n.*178+249_*178+250delinsCG
ENST00000348035.9:c.225+249_225+250delinsCG MANE Select	ENSP00000258737.7:n.225+249_225+250delinsCG
ENST00000348035.8:c.225+249_225+250delinsCG	ENSP00000258737.7:n.225+249_225+250delinsCG
ENST00000356142.4:c.225+249_225+250delinsCG	ENSP00000348461.4:n.225+249_225+250delinsCG
ENST00000488373.5:n.456+249_456+250delinsCG
ENST00000497741.5:n.241+249_241+250delinsCG
NM_006908.4:c.225+249_225+250delinsCG	NP_008839.2:n.225+249_225+250delinsCG
NM_018890.3:c.225+249_225+250delinsCG	NP_061485.1:n.225+249_225+250delinsCG
NM_006908.5:c.225+249_225+250delinsCG MANE Select	NP_008839.2:n.225+249_225+250delinsCG
NM_018890.4:c.225+249_225+250delinsCG	NP_061485.1:n.225+249_225+250delinsCG