Canonical Allele Identifier: CA1685476793
Gene: RAC1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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