Canonical Allele Identifier: CA882866618
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs35048370
MyVariant Identifiers: chr19:g.47507176_47507193del (hg19) chr19:g.47003919_47003936del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003933_47003950del , CM000681.2:g.47003933_47003950del GRCh38
NC_000019.9:g.47507190_47507207del , CM000681.1:g.47507190_47507207del GRCh37
NC_000019.8:g.52199030_52199047del NCBI36
NG_047014.1:g.90367_90384del
NG_047014.2:g.147937_147954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7745_7762del ENSP00000385720.2:n.7745_7762del
ENST00000672722.1:c.*3245_*3262del MANE Select ENSP00000500409.1:n.*3245_*3262del
ENST00000404338.7:c.7745_7762del ENSP00000385720.2:n.7745_7762del
ENST00000614079.1:c.7322_7339del ENSP00000483730.1:n.7322_7339del
NM_004491.4:c.7745_7762del NP_004482.4:n.7745_7762del
NM_004491.5:c.*3245_*3262del MANE Select NP_004482.4:n.*3245_*3262del
Search 100 bp 5'
Search 100 bp 3'