Canonical Allele Identifier: CA309124036
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs34696151
MyVariant Identifiers: chr19:g.47507174del (hg19) chr19:g.47003917del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917del , CM000681.2:g.47003917del GRCh38
NC_000019.9:g.47507174del , CM000681.1:g.47507174del GRCh37
NC_000019.8:g.52199014del NCBI36
NG_047014.1:g.90351del
NG_047014.2:g.147921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729del ENSP00000385720.2:n.7729del
ENST00000672722.1:c.*3229del MANE Select ENSP00000500409.1:n.*3229del
ENST00000404338.7:c.7729del ENSP00000385720.2:n.7729del
ENST00000614079.1:c.7306del ENSP00000483730.1:n.7306del
NM_004491.4:c.7729del NP_004482.4:n.7729del
NM_004491.5:c.*3229del MANE Select NP_004482.4:n.*3229del
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