Canonical Allele Identifier: CA1158217452
Gene: CDC42 HGNC NCBI
CDC42-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22035262T= , CM000663.2:g.22035262T= GRCh38
NC_000001.10:g.22361755T= , CM000663.1:g.22361755T= GRCh37
NC_000001.9:g.22234342T= NCBI36
NG_047042.3:g.14752T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695855.1:c.-51+9890T= ENSP00000512220.1:n.-51+9890T=
ENST00000695856.1:c.-51+9623T= ENSP00000512221.1:n.-51+9623T=
ENST00000648594.1:c.-51+9623T= (CDC42) ENSP00000497733.1:n.-51+9623T=
XR_947048.1:n.84-3395A=
XR_002958282.1:n.141-3395A= (CDC42-AS1)