Canonical Allele Identifier: CA2586003830
Gene: ARHGAP35 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003949_47003952del , CM000681.2:g.47003949_47003952del GRCh38
NC_000019.9:g.47507206_47507209del , CM000681.1:g.47507206_47507209del GRCh37
NC_000019.8:g.52199046_52199049del NCBI36
NG_047014.1:g.90383_90386del
NG_047014.2:g.147953_147956del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7761_7764del ENSP00000385720.2:n.7761_7764del
ENST00000672722.1:c.*3261_*3264del MANE Select ENSP00000500409.1:n.*3261_*3264del
ENST00000404338.7:c.7761_7764del ENSP00000385720.2:n.7761_7764del
ENST00000614079.1:c.7338_7341del ENSP00000483730.1:n.7338_7341del
NM_004491.4:c.7761_7764del NP_004482.4:n.7761_7764del
NM_004491.5:c.*3261_*3264del MANE Select NP_004482.4:n.*3261_*3264del