Canonical Allele Identifier: CA2614979034
Gene: ARAP1 HGNC NCBI

Linked Data

gnomAD v4: 11-72722368-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722373del , CM000673.2:g.72722373del GRCh38
NC_000011.9:g.72433418del , CM000673.1:g.72433418del GRCh37
NC_000011.8:g.72111066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4251del MANE Select ENSP00000377233.3:n.509+4251del
ENST00000359373.9:c.509+4251del ENSP00000352332.5:n.509+4251del
ENST00000393609.7:c.509+4251del ENSP00000377233.3:n.509+4251del
NM_001040118.2:c.509+4251del NP_001035207.1:n.509+4251del
NM_001040118.3:c.509+4251del MANE Select NP_001035207.1:n.509+4251del
Search 100 bp 5'
Search 100 bp 3'