Canonical Allele Identifier: CA2586004308

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47004388-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004389del , CM000681.2:g.47004389del	GRCh38
NC_000019.9:g.47507646del , CM000681.1:g.47507646del	GRCh37
NC_000019.8:g.52199486del	NCBI36
NG_047014.1:g.90823del
NG_047014.2:g.148393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8201del	ENSP00000385720.2:n.8201del
ENST00000672722.1:c.*3701del MANE Select	ENSP00000500409.1:n.*3701del
ENST00000404338.7:c.8201del	ENSP00000385720.2:n.8201del
NM_004491.4:c.8201del	NP_004482.4:n.8201del
NM_004491.5:c.*3701del MANE Select	NP_004482.4:n.*3701del