Canonical Allele Identifier: CA2580617501

Gene: RAC1

Linked Data

• ClinVar Variation Id: 2577934
• ClinVar RCV Id: RCV003325340

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.6391938_6391939delinsAC , CM000669.2:g.6391938_6391939delinsAC	GRCh38
NC_000007.13:g.6431569_6431570delinsAC , CM000669.1:g.6431569_6431570delinsAC	GRCh37
NC_000007.12:g.6398094_6398095delinsAC	NCBI36
NG_029431.1:g.22444_22445delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696666.1:n.310_311delinsAC
ENST00000704002.1:c.221_222delinsAC	ENSP00000515615.1:p.Ser74Tyr
ENST00000704003.1:c.*75_*76delinsAC	ENSP00000515616.1:n.*75_*76delinsAC
ENST00000348035.9:c.122_123delinsAC MANE Select	ENSP00000258737.7:p.Ser41Tyr
ENST00000348035.8:c.122_123delinsAC	ENSP00000258737.7:p.Ser41Tyr
ENST00000356142.4:c.122_123delinsAC	ENSP00000348461.4:p.Ser41Tyr
ENST00000488373.5:n.353_354delinsAC
ENST00000497741.5:n.138_139delinsAC
NM_006908.4:c.122_123delinsAC	NP_008839.2:p.Ser41Tyr
NM_018890.3:c.122_123delinsAC	NP_061485.1:p.Ser41Tyr
NM_006908.5:c.122_123delinsAC MANE Select	NP_008839.2:p.Ser41Tyr
NM_018890.4:c.122_123delinsAC	NP_061485.1:p.Ser41Tyr