Canonical Allele Identifier: CA2574916196
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722392_72722393del , CM000673.2:g.72722392_72722393del GRCh38
NC_000011.9:g.72433437_72433438del , CM000673.1:g.72433437_72433438del GRCh37
NC_000011.8:g.72111085_72111086del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4229_509+4230del MANE Select ENSP00000377233.3:n.509+4229_509+4230del
ENST00000359373.9:c.509+4229_509+4230del ENSP00000352332.5:n.509+4229_509+4230del
ENST00000393609.7:c.509+4229_509+4230del ENSP00000377233.3:n.509+4229_509+4230del
NM_001040118.2:c.509+4229_509+4230del NP_001035207.1:n.509+4229_509+4230del
NM_001040118.3:c.509+4229_509+4230del MANE Select NP_001035207.1:n.509+4229_509+4230del