Canonical Allele Identifier: CA309124536

Gene: ARHGAP35

Linked Data

• dbSNP Id: rs386809896

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004385_47004386delinsCT , CM000681.2:g.47004385_47004386delinsCT	GRCh38
NC_000019.9:g.47507642_47507643delinsCT , CM000681.1:g.47507642_47507643delinsCT	GRCh37
NC_000019.8:g.52199482_52199483delinsCT	NCBI36
NG_047014.1:g.90819_90820delinsCT
NG_047014.2:g.148389_148390delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8197_8198delinsCT	ENSP00000385720.2:n.8197_8198delinsCT
ENST00000672722.1:c.*3697_*3698delinsCT MANE Select	ENSP00000500409.1:n.*3697_*3698delinsCT
ENST00000404338.7:c.8197_8198delinsCT	ENSP00000385720.2:n.8197_8198delinsCT
NM_004491.4:c.8197_8198delinsCT	NP_004482.4:n.8197_8198delinsCT
NM_004491.5:c.*3697_*3698delinsCT MANE Select	NP_004482.4:n.*3697_*3698delinsCT