Canonical Allele Identifier: CA1139942229
Gene: CDC42 HGNC NCBI
CDC42-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22047131C= , CM000663.2:g.22047131C= GRCh38
NC_000001.10:g.22373624C= , CM000663.1:g.22373624C= GRCh37
NC_000001.9:g.22246211C= NCBI36
NG_047042.3:g.26621C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695855.1:c.-51+21759C= ENSP00000512220.1:n.-51+21759C=
ENST00000695856.1:c.-51+21492C= ENSP00000512221.1:n.-51+21492C=
ENST00000648594.1:c.-51+21492C= (CDC42) ENSP00000497733.1:n.-51+21492C=
XR_947048.1:n.83+5656G=
XR_002958282.1:n.140+5656G= (CDC42-AS1)