Canonical Allele Identifier: CA2339183442
Gene: ARHGAP35 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003916_47003917delinsAC , CM000681.2:g.47003916_47003917delinsAC GRCh38
NC_000019.9:g.47507173_47507174delinsAC , CM000681.1:g.47507173_47507174delinsAC GRCh37
NC_000019.8:g.52199013_52199014delinsAC NCBI36
NG_047014.1:g.90350_90351delinsAC
NG_047014.2:g.147920_147921delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7728_7729delinsAC ENSP00000385720.2:n.7728_7729delinsAC
ENST00000672722.1:c.*3228_*3229delinsAC MANE Select ENSP00000500409.1:n.*3228_*3229delinsAC
ENST00000404338.7:c.7728_7729delinsAC ENSP00000385720.2:n.7728_7729delinsAC
ENST00000614079.1:c.7305_7306delinsAC ENSP00000483730.1:n.7305_7306delinsAC
NM_004491.4:c.7728_7729delinsAC NP_004482.4:n.7728_7729delinsAC
NM_004491.5:c.*3228_*3229delinsAC MANE Select NP_004482.4:n.*3228_*3229delinsAC