Canonical Allele Identifier: CA2339183402

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003851G= , CM000681.2:g.47003851G=	GRCh38
NC_000019.9:g.47507108G= , CM000681.1:g.47507108G=	GRCh37
NC_000019.8:g.52198948G=	NCBI36
NG_047014.1:g.90285G=
NG_047014.2:g.147855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7663G=	ENSP00000385720.2:n.7663G=
ENST00000672722.1:c.*3163G= MANE Select	ENSP00000500409.1:n.*3163G=
ENST00000404338.7:c.7663G=	ENSP00000385720.2:n.7663G=
ENST00000614079.1:c.7240G=	ENSP00000483730.1:n.7240G=
NM_004491.4:c.7663G=	NP_004482.4:n.7663G=
NM_004491.5:c.*3163G= MANE Select	NP_004482.4:n.*3163G=