Canonical Allele Identifier: CA153350338
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1020636889
gnomAD v2: 7-6431534-C-T
gnomAD v3: 7-6391903-C-T
gnomAD v4: 7-6391903-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6391903C>T , CM000669.2:g.6391903C>T GRCh38
NC_000007.13:g.6431534C>T , CM000669.1:g.6431534C>T GRCh37
NC_000007.12:g.6398059C>T NCBI36
NG_029431.1:g.22409C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.296-21C>T
ENST00000704002.1:c.207-21C>T ENSP00000515615.1:n.207-21C>T
ENST00000704003.1:c.*61-21C>T ENSP00000515616.1:n.*61-21C>T
ENST00000348035.9:c.108-21C>T MANE Select ENSP00000258737.7:n.108-21C>T
ENST00000348035.8:c.108-21C>T ENSP00000258737.7:n.108-21C>T
ENST00000356142.4:c.108-21C>T ENSP00000348461.4:n.108-21C>T
ENST00000488373.5:n.339-21C>T
ENST00000497741.5:n.124-21C>T
NM_006908.4:c.108-21C>T NP_008839.2:n.108-21C>T
NM_018890.3:c.108-21C>T NP_061485.1:n.108-21C>T
NM_006908.5:c.108-21C>T MANE Select NP_008839.2:n.108-21C>T
NM_018890.4:c.108-21C>T NP_061485.1:n.108-21C>T