Canonical Allele Identifier: CA2586003662
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003847-GA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003850del , CM000681.2:g.47003850del GRCh38
NC_000019.9:g.47507107del , CM000681.1:g.47507107del GRCh37
NC_000019.8:g.52198947del NCBI36
NG_047014.1:g.90284del
NG_047014.2:g.147854del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7662del ENSP00000385720.2:n.7662del
ENST00000672722.1:c.*3162del MANE Select ENSP00000500409.1:n.*3162del
ENST00000404338.7:c.7662del ENSP00000385720.2:n.7662del
ENST00000614079.1:c.7239del ENSP00000483730.1:n.7239del
NM_004491.4:c.7662del NP_004482.4:n.7662del
NM_004491.5:c.*3162del MANE Select NP_004482.4:n.*3162del
Search 100 bp 5'
Search 100 bp 3'