Canonical Allele Identifier: CA309124040
Gene: ARHGAP35 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.47507174_47507175insCG (hg19) chr19:g.47003917_47003918insCG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003917_47003918insCG , CM000681.2:g.47003917_47003918insCG GRCh38
NC_000019.9:g.47507174_47507175insCG , CM000681.1:g.47507174_47507175insCG GRCh37
NC_000019.8:g.52199014_52199015insCG NCBI36
NG_047014.1:g.90351_90352insCG
NG_047014.2:g.147921_147922insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7729_7730insCG ENSP00000385720.2:n.7729_7730insCG
ENST00000672722.1:c.*3229_*3230insCG MANE Select ENSP00000500409.1:n.*3229_*3230insCG
ENST00000404338.7:c.7729_7730insCG ENSP00000385720.2:n.7729_7730insCG
ENST00000614079.1:c.7306_7307insCG ENSP00000483730.1:n.7306_7307insCG
NM_004491.4:c.7729_7730insCG NP_004482.4:n.7729_7730insCG
NM_004491.5:c.*3229_*3230insCG MANE Select NP_004482.4:n.*3229_*3230insCG
Search 100 bp 5'
Search 100 bp 3'