Canonical Allele Identifier: CA2339183770

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004392C= , CM000681.2:g.47004392C=	GRCh38
NC_000019.9:g.47507649C= , CM000681.1:g.47507649C=	GRCh37
NC_000019.8:g.52199489C=	NCBI36
NG_047014.1:g.90826C=
NG_047014.2:g.148396C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8204C=	ENSP00000385720.2:n.8204C=
ENST00000672722.1:c.*3704C= MANE Select	ENSP00000500409.1:n.*3704C=
ENST00000404338.7:c.8204C=	ENSP00000385720.2:n.8204C=
NM_004491.4:c.8204C=	NP_004482.4:n.8204C=
NM_004491.5:c.*3704C= MANE Select	NP_004482.4:n.*3704C=