Canonical Allele Identifier: CA2339183727

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004341G= , CM000681.2:g.47004341G=	GRCh38
NC_000019.9:g.47507598G= , CM000681.1:g.47507598G=	GRCh37
NC_000019.8:g.52199438G=	NCBI36
NG_047014.1:g.90775G=
NG_047014.2:g.148345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8153G=	ENSP00000385720.2:n.8153G=
ENST00000672722.1:c.*3653G= MANE Select	ENSP00000500409.1:n.*3653G=
ENST00000404338.7:c.8153G=	ENSP00000385720.2:n.8153G=
NM_004491.4:c.8153G=	NP_004482.4:n.8153G=
NM_004491.5:c.*3653G= MANE Select	NP_004482.4:n.*3653G=