Canonical Allele Identifier: CA309124063

Gene: ARHGAP35

Linked Data

• dbSNP Id: rs35048370
• gnomAD v2: 19-47507175-G-GCACA
• gnomAD v3: 19-47003918-G-GCACA
• gnomAD v4: 19-47003918-G-GCACA
• MyVariant Identifiers: chr19:g.47507177_47507178insCACA (hg19) ; chr19:g.47507175_47507176insCACA (hg19) ; chr19:g.47003920_47003921insCACA (hg38) ; chr19:g.47003918_47003919insCACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003947_47003950dup , CM000681.2:g.47003947_47003950dup	GRCh38
NC_000019.9:g.47507204_47507207dup , CM000681.1:g.47507204_47507207dup	GRCh37
NC_000019.8:g.52199044_52199047dup	NCBI36
NG_047014.1:g.90381_90384dup
NG_047014.2:g.147951_147954dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7759_7762dup	ENSP00000385720.2:n.7759_7762dup
ENST00000672722.1:c.*3259_*3262dup MANE Select	ENSP00000500409.1:n.*3259_*3262dup
ENST00000404338.7:c.7759_7762dup	ENSP00000385720.2:n.7759_7762dup
ENST00000614079.1:c.7336_7339dup	ENSP00000483730.1:n.7336_7339dup
NM_004491.4:c.7759_7762dup	NP_004482.4:n.7759_7762dup
NM_004491.5:c.*3259_*3262dup MANE Select	NP_004482.4:n.*3259_*3262dup