Canonical Allele Identifier: CA1982116620
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721677_72721680delinsGAGA , CM000673.2:g.72721677_72721680delinsGAGA GRCh38
NC_000011.9:g.72432722_72432725delinsGAGA , CM000673.1:g.72432722_72432725delinsGAGA GRCh37
NC_000011.8:g.72110370_72110373delinsGAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4940_509+4943delinsTCTC MANE Select ENSP00000377233.3:n.509+4940_509+4943delinsTCTC
ENST00000334211.12:c.-227+170_-227+173delinsTCTC ENSP00000335506.8:n.-227+170_-227+173delinsTCTC
ENST00000359373.9:c.509+4940_509+4943delinsTCTC ENSP00000352332.5:n.509+4940_509+4943delinsTCTC
ENST00000393609.7:c.509+4940_509+4943delinsTCTC ENSP00000377233.3:n.509+4940_509+4943delinsTCTC
ENST00000426523.5:c.-227+170_-227+173delinsTCTC ENSP00000392264.1:n.-227+170_-227+173delinsTCTC
ENST00000429686.5:c.-227+170_-227+173delinsTCTC ENSP00000403127.1:n.-227+170_-227+173delinsTCTC
ENST00000465814.5:n.239+170_239+173delinsTCTC
NM_001040118.2:c.509+4940_509+4943delinsTCTC NP_001035207.1:n.509+4940_509+4943delinsTCTC
NM_001135190.1:c.-227+170_-227+173delinsTCTC NP_001128662.1:n.-227+170_-227+173delinsTCTC
NM_015242.4:c.-227+170_-227+173delinsTCTC NP_056057.2:n.-227+170_-227+173delinsTCTC
NM_001369489.1:c.-227+170_-227+173delinsTCTC NP_001356418.1:n.-227+170_-227+173delinsTCTC
NR_161388.1:n.491+170_491+173delinsTCTC
NM_001040118.3:c.509+4940_509+4943delinsTCTC MANE Select NP_001035207.1:n.509+4940_509+4943delinsTCTC
NM_001135190.2:c.-227+170_-227+173delinsTCTC NP_001128662.1:n.-227+170_-227+173delinsTCTC
NM_015242.5:c.-227+170_-227+173delinsTCTC NP_056057.2:n.-227+170_-227+173delinsTCTC