Canonical Allele Identifier: CA2586003779
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003918-G-GTA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003918_47003919insTA , CM000681.2:g.47003918_47003919insTA GRCh38
NC_000019.9:g.47507175_47507176insTA , CM000681.1:g.47507175_47507176insTA GRCh37
NC_000019.8:g.52199015_52199016insTA NCBI36
NG_047014.1:g.90352_90353insTA
NG_047014.2:g.147922_147923insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7730_7731insTA ENSP00000385720.2:n.7730_7731insTA
ENST00000672722.1:c.*3230_*3231insTA MANE Select ENSP00000500409.1:n.*3230_*3231insTA
ENST00000404338.7:c.7730_7731insTA ENSP00000385720.2:n.7730_7731insTA
ENST00000614079.1:c.7307_7308insTA ENSP00000483730.1:n.7307_7308insTA
NM_004491.4:c.7730_7731insTA NP_004482.4:n.7730_7731insTA
NM_004491.5:c.*3230_*3231insTA MANE Select NP_004482.4:n.*3230_*3231insTA
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