Canonical Allele Identifier: CA2339183611

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004167A= , CM000681.2:g.47004167A=	GRCh38
NC_000019.9:g.47507424A= , CM000681.1:g.47507424A=	GRCh37
NC_000019.8:g.52199264A=	NCBI36
NG_047014.1:g.90601A=
NG_047014.2:g.148171A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7979A=	ENSP00000385720.2:n.7979A=
ENST00000672722.1:c.*3479A= MANE Select	ENSP00000500409.1:n.*3479A=
ENST00000404338.7:c.7979A=	ENSP00000385720.2:n.7979A=
ENST00000614079.1:c.7556A=	ENSP00000483730.1:n.7556A=
NM_004491.4:c.7979A=	NP_004482.4:n.7979A=
NM_004491.5:c.*3479A= MANE Select	NP_004482.4:n.*3479A=