Canonical Allele Identifier: CA1685476794
Gene: RAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1783108571

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392182C>T , CM000669.2:g.6392182C>T GRCh38
NC_000007.13:g.6431813C>T , CM000669.1:g.6431813C>T GRCh37
NC_000007.12:g.6398338C>T NCBI36
NG_029431.1:g.22688C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.554C>T
ENST00000704002.1:c.324+141C>T ENSP00000515615.1:n.324+141C>T
ENST00000704003.1:c.*178+141C>T ENSP00000515616.1:n.*178+141C>T
ENST00000348035.9:c.225+141C>T MANE Select ENSP00000258737.7:n.225+141C>T
ENST00000348035.8:c.225+141C>T ENSP00000258737.7:n.225+141C>T
ENST00000356142.4:c.225+141C>T ENSP00000348461.4:n.225+141C>T
ENST00000488373.5:n.456+141C>T
ENST00000497741.5:n.241+141C>T
NM_006908.4:c.225+141C>T NP_008839.2:n.225+141C>T
NM_018890.3:c.225+141C>T NP_061485.1:n.225+141C>T
NM_006908.5:c.225+141C>T MANE Select NP_008839.2:n.225+141C>T
NM_018890.4:c.225+141C>T NP_061485.1:n.225+141C>T