Canonical Allele Identifier: CA2339183562

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004095C= , CM000681.2:g.47004095C=	GRCh38
NC_000019.9:g.47507352C= , CM000681.1:g.47507352C=	GRCh37
NC_000019.8:g.52199192C=	NCBI36
NG_047014.1:g.90529C=
NG_047014.2:g.148099C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000404338.8:c.7907C=	ENSP00000385720.2:n.7907C=
ENST00000672722.1:c.*3407C= MANE Select	ENSP00000500409.1:n.*3407C=
ENST00000404338.7:c.7907C=	ENSP00000385720.2:n.7907C=
ENST00000614079.1:c.7484C=	ENSP00000483730.1:n.7484C=
NM_004491.4:c.7907C=	NP_004482.4:n.7907C=
NM_004491.5:c.*3407C= MANE Select	NP_004482.4:n.*3407C=