Canonical Allele Identifier: CA2586003672
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003858-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003861del , CM000681.2:g.47003861del GRCh38
NC_000019.9:g.47507118del , CM000681.1:g.47507118del GRCh37
NC_000019.8:g.52198958del NCBI36
NG_047014.1:g.90295del
NG_047014.2:g.147865del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7673del ENSP00000385720.2:n.7673del
ENST00000672722.1:c.*3173del MANE Select ENSP00000500409.1:n.*3173del
ENST00000404338.7:c.7673del ENSP00000385720.2:n.7673del
ENST00000614079.1:c.7250del ENSP00000483730.1:n.7250del
NM_004491.4:c.7673del NP_004482.4:n.7673del
NM_004491.5:c.*3173del MANE Select NP_004482.4:n.*3173del
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