Canonical Allele Identifier: CA2792663997
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722157del , CM000673.2:g.72722157del GRCh38
NC_000011.9:g.72433202del , CM000673.1:g.72433202del GRCh37
NC_000011.8:g.72110850del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4463del MANE Select ENSP00000377233.3:n.509+4463del
ENST00000334211.12:c.-534del ENSP00000335506.8:n.-534del
ENST00000359373.9:c.509+4463del ENSP00000352332.5:n.509+4463del
ENST00000393609.7:c.509+4463del ENSP00000377233.3:n.509+4463del
NM_001040118.2:c.509+4463del NP_001035207.1:n.509+4463del
NM_001135190.1:c.-534del NP_001128662.1:n.-534del
NM_015242.4:c.-534del NP_056057.2:n.-534del
NM_001369489.1:c.-534del NP_001356418.1:n.-534del
NR_161388.1:n.184del
NM_001040118.3:c.509+4463del MANE Select NP_001035207.1:n.509+4463del
NM_001135190.2:c.-534del NP_001128662.1:n.-534del
NM_015242.5:c.-534del NP_056057.2:n.-534del