Canonical Allele Identifier: CA2586003695

Gene: ARHGAP35

Linked Data

• gnomAD v4: 19-47003877-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003877_47003878insA , CM000681.2:g.47003877_47003878insA	GRCh38
NC_000019.9:g.47507134_47507135insA , CM000681.1:g.47507134_47507135insA	GRCh37
NC_000019.8:g.52198974_52198975insA	NCBI36
NG_047014.1:g.90311_90312insA
NG_047014.2:g.147881_147882insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7689_7690insA	ENSP00000385720.2:n.7689_7690insA
ENST00000672722.1:c.*3189_*3190insA MANE Select	ENSP00000500409.1:n.*3189_*3190insA
ENST00000404338.7:c.7689_7690insA	ENSP00000385720.2:n.7689_7690insA
ENST00000614079.1:c.7266_7267insA	ENSP00000483730.1:n.7266_7267insA
NM_004491.4:c.7689_7690insA	NP_004482.4:n.7689_7690insA
NM_004491.5:c.*3189_*3190insA MANE Select	NP_004482.4:n.*3189_*3190insA