Canonical Allele Identifier: CA309124136
Gene: ARHGAP35 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.47507176_47507177insCA (hg19) chr19:g.47003919_47003920insCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003919_47003920insCA , CM000681.2:g.47003919_47003920insCA GRCh38
NC_000019.9:g.47507176_47507177insCA , CM000681.1:g.47507176_47507177insCA GRCh37
NC_000019.8:g.52199016_52199017insCA NCBI36
NG_047014.1:g.90353_90354insCA
NG_047014.2:g.147923_147924insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7731_7732insCA ENSP00000385720.2:n.7731_7732insCA
ENST00000672722.1:c.*3231_*3232insCA MANE Select ENSP00000500409.1:n.*3231_*3232insCA
ENST00000404338.7:c.7731_7732insCA ENSP00000385720.2:n.7731_7732insCA
ENST00000614079.1:c.7308_7309insCA ENSP00000483730.1:n.7308_7309insCA
NM_004491.4:c.7731_7732insCA NP_004482.4:n.7731_7732insCA
NM_004491.5:c.*3231_*3232insCA MANE Select NP_004482.4:n.*3231_*3232insCA
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