Canonical Allele Identifier: CA882866660
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1383504002
MyVariant Identifiers: chr19:g.47507184_47507185insAT (hg19) chr19:g.47003927_47003928insAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003928_47003929insTA , CM000681.2:g.47003928_47003929insTA GRCh38
NC_000019.9:g.47507185_47507186insTA , CM000681.1:g.47507185_47507186insTA GRCh37
NC_000019.8:g.52199025_52199026insTA NCBI36
NG_047014.1:g.90362_90363insTA
NG_047014.2:g.147932_147933insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7740_7741insTA ENSP00000385720.2:n.7740_7741insTA
ENST00000672722.1:c.*3240_*3241insTA MANE Select ENSP00000500409.1:n.*3240_*3241insTA
ENST00000404338.7:c.7740_7741insTA ENSP00000385720.2:n.7740_7741insTA
ENST00000614079.1:c.7317_7318insTA ENSP00000483730.1:n.7317_7318insTA
NM_004491.4:c.7740_7741insTA NP_004482.4:n.7740_7741insTA
NM_004491.5:c.*3240_*3241insTA MANE Select NP_004482.4:n.*3240_*3241insTA
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