Canonical Allele Identifier: CA1982117059
Gene: ARAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722484A= , CM000673.2:g.72722484A= GRCh38
NC_000011.9:g.72433529A= , CM000673.1:g.72433529A= GRCh37
NC_000011.8:g.72111177A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4136T= MANE Select ENSP00000377233.3:n.509+4136T=
ENST00000359373.9:c.509+4136T= ENSP00000352332.5:n.509+4136T=
ENST00000393609.7:c.509+4136T= ENSP00000377233.3:n.509+4136T=
NM_001040118.2:c.509+4136T= NP_001035207.1:n.509+4136T=
NM_001040118.3:c.509+4136T= MANE Select NP_001035207.1:n.509+4136T=
Search 100 bp 5'
Search 100 bp 3'