Canonical Allele Identifier: CA2339183761
Gene: ARHGAP35 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004374_47004375delinsAC , CM000681.2:g.47004374_47004375delinsAC GRCh38
NC_000019.9:g.47507631_47507632delinsAC , CM000681.1:g.47507631_47507632delinsAC GRCh37
NC_000019.8:g.52199471_52199472delinsAC NCBI36
NG_047014.1:g.90808_90809delinsAC
NG_047014.2:g.148378_148379delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8186_8187delinsAC ENSP00000385720.2:n.8186_8187delinsAC
ENST00000672722.1:c.*3686_*3687delinsAC MANE Select ENSP00000500409.1:n.*3686_*3687delinsAC
ENST00000404338.7:c.8186_8187delinsAC ENSP00000385720.2:n.8186_8187delinsAC
NM_004491.4:c.8186_8187delinsAC NP_004482.4:n.8186_8187delinsAC
NM_004491.5:c.*3686_*3687delinsAC MANE Select NP_004482.4:n.*3686_*3687delinsAC
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