Canonical Allele Identifier: CA2792663980
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721768_72721769insGTCGCCGTATCATT , CM000673.2:g.72721768_72721769insGTCGCCGTATCATT GRCh38
NC_000011.9:g.72432813_72432814insGTCGCCGTATCATT , CM000673.1:g.72432813_72432814insGTCGCCGTATCATT GRCh37
NC_000011.8:g.72110461_72110462insGTCGCCGTATCATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4851_509+4852insAATGATACGGCGAC MANE Select ENSP00000377233.3:n.509+4851_509+4852insAATGATACGGCGAC
ENST00000334211.12:c.-227+81_-227+82insAATGATACGGCGAC ENSP00000335506.8:n.-227+81_-227+82insAATGATACGGCGAC
ENST00000359373.9:c.509+4851_509+4852insAATGATACGGCGAC ENSP00000352332.5:n.509+4851_509+4852insAATGATACGGCGAC
ENST00000393609.7:c.509+4851_509+4852insAATGATACGGCGAC ENSP00000377233.3:n.509+4851_509+4852insAATGATACGGCGAC
ENST00000426523.5:c.-227+81_-227+82insAATGATACGGCGAC ENSP00000392264.1:n.-227+81_-227+82insAATGATACGGCGAC
ENST00000429686.5:c.-227+81_-227+82insAATGATACGGCGAC ENSP00000403127.1:n.-227+81_-227+82insAATGATACGGCGAC
ENST00000465814.5:n.239+81_239+82insAATGATACGGCGAC
NM_001040118.2:c.509+4851_509+4852insAATGATACGGCGAC NP_001035207.1:n.509+4851_509+4852insAATGATACGGCGAC
NM_001135190.1:c.-227+81_-227+82insAATGATACGGCGAC NP_001128662.1:n.-227+81_-227+82insAATGATACGGCGAC
NM_015242.4:c.-227+81_-227+82insAATGATACGGCGAC NP_056057.2:n.-227+81_-227+82insAATGATACGGCGAC
NM_001369489.1:c.-227+81_-227+82insAATGATACGGCGAC NP_001356418.1:n.-227+81_-227+82insAATGATACGGCGAC
NR_161388.1:n.491+81_491+82insAATGATACGGCGAC
NM_001040118.3:c.509+4851_509+4852insAATGATACGGCGAC MANE Select NP_001035207.1:n.509+4851_509+4852insAATGATACGGCGAC
NM_001135190.2:c.-227+81_-227+82insAATGATACGGCGAC NP_001128662.1:n.-227+81_-227+82insAATGATACGGCGAC
NM_015242.5:c.-227+81_-227+82insAATGATACGGCGAC NP_056057.2:n.-227+81_-227+82insAATGATACGGCGAC