Canonical Allele Identifier: CA2814602912

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004310_47004311del , CM000681.2:g.47004310_47004311del	GRCh38
NC_000019.9:g.47507567_47507568del , CM000681.1:g.47507567_47507568del	GRCh37
NC_000019.8:g.52199407_52199408del	NCBI36
NG_047014.1:g.90744_90745del
NG_047014.2:g.148314_148315del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8122_8123del	ENSP00000385720.2:n.8122_8123del
ENST00000672722.1:c.*3622_*3623del MANE Select	ENSP00000500409.1:n.*3622_*3623del
ENST00000404338.7:c.8122_8123del	ENSP00000385720.2:n.8122_8123del
NM_004491.4:c.8122_8123del	NP_004482.4:n.8122_8123del
NM_004491.5:c.*3622_*3623del MANE Select	NP_004482.4:n.*3622_*3623del