Canonical Allele Identifier: CA2339183728

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004342C= , CM000681.2:g.47004342C=	GRCh38
NC_000019.9:g.47507599C= , CM000681.1:g.47507599C=	GRCh37
NC_000019.8:g.52199439C=	NCBI36
NG_047014.1:g.90776C=
NG_047014.2:g.148346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8154C=	ENSP00000385720.2:n.8154C=
ENST00000672722.1:c.*3654C= MANE Select	ENSP00000500409.1:n.*3654C=
ENST00000404338.7:c.8154C=	ENSP00000385720.2:n.8154C=
NM_004491.4:c.8154C=	NP_004482.4:n.8154C=
NM_004491.5:c.*3654C= MANE Select	NP_004482.4:n.*3654C=