Canonical Allele Identifier: CA882866908
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1408493618
MyVariant Identifiers: chr19:g.47507595_47507596insGC (hg19) chr19:g.47004338_47004339insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004346_47004347dup , CM000681.2:g.47004346_47004347dup GRCh38
NC_000019.9:g.47507603_47507604dup , CM000681.1:g.47507603_47507604dup GRCh37
NC_000019.8:g.52199443_52199444dup NCBI36
NG_047014.1:g.90780_90781dup
NG_047014.2:g.148350_148351dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8158_8159dup ENSP00000385720.2:n.8158_8159dup
ENST00000672722.1:c.*3658_*3659dup MANE Select ENSP00000500409.1:n.*3658_*3659dup
ENST00000404338.7:c.8158_8159dup ENSP00000385720.2:n.8158_8159dup
NM_004491.4:c.8158_8159dup NP_004482.4:n.8158_8159dup
NM_004491.5:c.*3658_*3659dup MANE Select NP_004482.4:n.*3658_*3659dup
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