Canonical Allele Identifier: CA2339183733

Gene: ARHGAP35

Linked Data

• dbSNP Id: rs2056765046

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004349_47004351dup , CM000681.2:g.47004349_47004351dup	GRCh38
NC_000019.9:g.47507606_47507608dup , CM000681.1:g.47507606_47507608dup	GRCh37
NC_000019.8:g.52199446_52199448dup	NCBI36
NG_047014.1:g.90783_90785dup
NG_047014.2:g.148353_148355dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8161_8163dup	ENSP00000385720.2:n.8161_8163dup
ENST00000672722.1:c.*3661_*3663dup MANE Select	ENSP00000500409.1:n.*3661_*3663dup
ENST00000404338.7:c.8161_8163dup	ENSP00000385720.2:n.8161_8163dup
NM_004491.4:c.8161_8163dup	NP_004482.4:n.8161_8163dup
NM_004491.5:c.*3661_*3663dup MANE Select	NP_004482.4:n.*3661_*3663dup