Canonical Allele Identifier: CA2339183435

Gene: ARHGAP35

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003913_47003931delinsGACACGCACACACACACAC , CM000681.2:g.47003913_47003931delinsGACACGCACACACACACAC	GRCh38
NC_000019.9:g.47507170_47507188delinsGACACGCACACACACACAC , CM000681.1:g.47507170_47507188delinsGACACGCACACACACACAC	GRCh37
NC_000019.8:g.52199010_52199028delinsGACACGCACACACACACAC	NCBI36
NG_047014.1:g.90347_90365delinsGACACGCACACACACACAC
NG_047014.2:g.147917_147935delinsGACACGCACACACACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7725_7743delinsGACACGCACACACACACAC	ENSP00000385720.2:n.7725_7743delinsGACACGCACACACACACAC
ENST00000672722.1:c.*3225_*3243delinsGACACGCACACACACACAC MANE Select	ENSP00000500409.1:n.*3225_*3243delinsGACACGCACACACACACAC
ENST00000404338.7:c.7725_7743delinsGACACGCACACACACACAC	ENSP00000385720.2:n.7725_7743delinsGACACGCACACACACACAC
ENST00000614079.1:c.7302_7320delinsGACACGCACACACACACAC	ENSP00000483730.1:n.7302_7320delinsGACACGCACACACACACAC
NM_004491.4:c.7725_7743delinsGACACGCACACACACACAC	NP_004482.4:n.7725_7743delinsGACACGCACACACACACAC
NM_004491.5:c.*3225_*3243delinsGACACGCACACACACACAC MANE Select	NP_004482.4:n.*3225_*3243delinsGACACGCACACACACACAC