Canonical Allele Identifier: CA2339183769

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004385_47004386delinsTG , CM000681.2:g.47004385_47004386delinsTG	GRCh38
NC_000019.9:g.47507642_47507643delinsTG , CM000681.1:g.47507642_47507643delinsTG	GRCh37
NC_000019.8:g.52199482_52199483delinsTG	NCBI36
NG_047014.1:g.90819_90820delinsTG
NG_047014.2:g.148389_148390delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8197_8198delinsTG	ENSP00000385720.2:n.8197_8198delinsTG
ENST00000672722.1:c.*3697_*3698delinsTG MANE Select	ENSP00000500409.1:n.*3697_*3698delinsTG
ENST00000404338.7:c.8197_8198delinsTG	ENSP00000385720.2:n.8197_8198delinsTG
NM_004491.4:c.8197_8198delinsTG	NP_004482.4:n.8197_8198delinsTG
NM_004491.5:c.*3697_*3698delinsTG MANE Select	NP_004482.4:n.*3697_*3698delinsTG