Canonical Allele Identifier: CA2339183441
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003916_47003918delinsACG , CM000681.2:g.47003916_47003918delinsACG GRCh38
NC_000019.9:g.47507173_47507175delinsACG , CM000681.1:g.47507173_47507175delinsACG GRCh37
NC_000019.8:g.52199013_52199015delinsACG NCBI36
NG_047014.1:g.90350_90352delinsACG
NG_047014.2:g.147920_147922delinsACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7728_7730delinsACG ENSP00000385720.2:n.7728_7730delinsACG
ENST00000672722.1:c.*3228_*3230delinsACG MANE Select ENSP00000500409.1:n.*3228_*3230delinsACG
ENST00000404338.7:c.7728_7730delinsACG ENSP00000385720.2:n.7728_7730delinsACG
ENST00000614079.1:c.7305_7307delinsACG ENSP00000483730.1:n.7305_7307delinsACG
NM_004491.4:c.7728_7730delinsACG NP_004482.4:n.7728_7730delinsACG
NM_004491.5:c.*3228_*3230delinsACG MANE Select NP_004482.4:n.*3228_*3230delinsACG