Canonical Allele Identifier: CA2586003780
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003923_47003950del , CM000681.2:g.47003923_47003950del GRCh38
NC_000019.9:g.47507180_47507207del , CM000681.1:g.47507180_47507207del GRCh37
NC_000019.8:g.52199020_52199047del NCBI36
NG_047014.1:g.90357_90384del
NG_047014.2:g.147927_147954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7735_7762del ENSP00000385720.2:n.7735_7762del
ENST00000672722.1:c.*3235_*3262del MANE Select ENSP00000500409.1:n.*3235_*3262del
ENST00000404338.7:c.7735_7762del ENSP00000385720.2:n.7735_7762del
ENST00000614079.1:c.7312_7339del ENSP00000483730.1:n.7312_7339del
NM_004491.4:c.7735_7762del NP_004482.4:n.7735_7762del
NM_004491.5:c.*3235_*3262del MANE Select NP_004482.4:n.*3235_*3262del