Canonical Allele Identifier: CA1685476754
Gene: RAC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.6392154G= , CM000669.2:g.6392154G= GRCh38
NC_000007.13:g.6431785G= , CM000669.1:g.6431785G= GRCh37
NC_000007.12:g.6398310G= NCBI36
NG_029431.1:g.22660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696666.1:n.526G=
ENST00000704002.1:c.324+113G= ENSP00000515615.1:n.324+113G=
ENST00000704003.1:c.*178+113G= ENSP00000515616.1:n.*178+113G=
ENST00000348035.9:c.225+113G= MANE Select ENSP00000258737.7:n.225+113G=
ENST00000348035.8:c.225+113G= ENSP00000258737.7:n.225+113G=
ENST00000356142.4:c.225+113G= ENSP00000348461.4:n.225+113G=
ENST00000488373.5:n.456+113G=
ENST00000497741.5:n.241+113G=
NM_006908.4:c.225+113G= NP_008839.2:n.225+113G=
NM_018890.3:c.225+113G= NP_061485.1:n.225+113G=
NM_006908.5:c.225+113G= MANE Select NP_008839.2:n.225+113G=
NM_018890.4:c.225+113G= NP_061485.1:n.225+113G=
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