Canonical Allele Identifier: CA2586003649
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003834-T-TTAAAAAA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003834_47003835insTAAAAAA , CM000681.2:g.47003834_47003835insTAAAAAA GRCh38
NC_000019.9:g.47507091_47507092insTAAAAAA , CM000681.1:g.47507091_47507092insTAAAAAA GRCh37
NC_000019.8:g.52198931_52198932insTAAAAAA NCBI36
NG_047014.1:g.90268_90269insTAAAAAA
NG_047014.2:g.147838_147839insTAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7646_7647insTAAAAAA ENSP00000385720.2:n.7646_7647insTAAAAAA
ENST00000672722.1:c.*3146_*3147insTAAAAAA MANE Select ENSP00000500409.1:n.*3146_*3147insTAAAAAA
ENST00000404338.7:c.7646_7647insTAAAAAA ENSP00000385720.2:n.7646_7647insTAAAAAA
ENST00000614079.1:c.7223_7224insTAAAAAA ENSP00000483730.1:n.7223_7224insTAAAAAA
NM_004491.4:c.7646_7647insTAAAAAA NP_004482.4:n.7646_7647insTAAAAAA
NM_004491.5:c.*3146_*3147insTAAAAAA MANE Select NP_004482.4:n.*3146_*3147insTAAAAAA
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