Canonical Allele Identifier: CA2339183492
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003982G= , CM000681.2:g.47003982G= GRCh38
NC_000019.9:g.47507239G= , CM000681.1:g.47507239G= GRCh37
NC_000019.8:g.52199079G= NCBI36
NG_047014.1:g.90416G=
NG_047014.2:g.147986G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7794G= ENSP00000385720.2:n.7794G=
ENST00000672722.1:c.*3294G= MANE Select ENSP00000500409.1:n.*3294G=
ENST00000404338.7:c.7794G= ENSP00000385720.2:n.7794G=
ENST00000614079.1:c.7371G= ENSP00000483730.1:n.7371G=
NM_004491.4:c.7794G= NP_004482.4:n.7794G=
NM_004491.5:c.*3294G= MANE Select NP_004482.4:n.*3294G=