Canonical Allele Identifier: CA2586003804

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003934-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003935_47003936insCC , CM000681.2:g.47003935_47003936insCC	GRCh38
NC_000019.9:g.47507192_47507193insCC , CM000681.1:g.47507192_47507193insCC	GRCh37
NC_000019.8:g.52199032_52199033insCC	NCBI36
NG_047014.1:g.90369_90370insCC
NG_047014.2:g.147939_147940insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7747_7748insCC	ENSP00000385720.2:n.7747_7748insCC
ENST00000672722.1:c.*3247_*3248insCC MANE Select	ENSP00000500409.1:n.*3247_*3248insCC
ENST00000404338.7:c.7747_7748insCC	ENSP00000385720.2:n.7747_7748insCC
ENST00000614079.1:c.7324_7325insCC	ENSP00000483730.1:n.7324_7325insCC
NM_004491.4:c.7747_7748insCC	NP_004482.4:n.7747_7748insCC
NM_004491.5:c.*3247_*3248insCC MANE Select	NP_004482.4:n.*3247_*3248insCC