Canonical Allele Identifier: CA2339183566
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004099_47004100delinsCG , CM000681.2:g.47004099_47004100delinsCG GRCh38
NC_000019.9:g.47507356_47507357delinsCG , CM000681.1:g.47507356_47507357delinsCG GRCh37
NC_000019.8:g.52199196_52199197delinsCG NCBI36
NG_047014.1:g.90533_90534delinsCG
NG_047014.2:g.148103_148104delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000404338.8:c.7911_7912delinsCG ENSP00000385720.2:n.7911_7912delinsCG
ENST00000672722.1:c.*3411_*3412delinsCG MANE Select ENSP00000500409.1:n.*3411_*3412delinsCG
ENST00000404338.7:c.7911_7912delinsCG ENSP00000385720.2:n.7911_7912delinsCG
ENST00000614079.1:c.7488_7489delinsCG ENSP00000483730.1:n.7488_7489delinsCG
NM_004491.4:c.7911_7912delinsCG NP_004482.4:n.7911_7912delinsCG
NM_004491.5:c.*3411_*3412delinsCG MANE Select NP_004482.4:n.*3411_*3412delinsCG