Canonical Allele Identifier: CA1685476442
Gene: RAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392035G= , CM000669.2:g.6392035G= GRCh38
NC_000007.13:g.6431666G= , CM000669.1:g.6431666G= GRCh37
NC_000007.12:g.6398191G= NCBI36
NG_029431.1:g.22541G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.407G=
ENST00000704002.1:c.318G= ENSP00000515615.1:p.Pro106=
ENST00000704003.1:c.*172G= ENSP00000515616.1:n.*172G=
ENST00000348035.9:c.219G= MANE Select ENSP00000258737.7:p.Pro73=
ENST00000348035.8:c.219G= ENSP00000258737.7:p.Pro73=
ENST00000356142.4:c.219G= ENSP00000348461.4:p.Pro73=
ENST00000488373.5:n.450G=
ENST00000497741.5:n.235G=
NM_006908.4:c.219G= NP_008839.2:p.Pro73=
NM_018890.3:c.219G= NP_061485.1:p.Pro73=
NM_006908.5:c.219G= MANE Select NP_008839.2:p.Pro73=
NM_018890.4:c.219G= NP_061485.1:p.Pro73=