Canonical Allele Identifier: CA1982116746
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721928G= , CM000673.2:g.72721928G= GRCh38
NC_000011.9:g.72432973G= , CM000673.1:g.72432973G= GRCh37
NC_000011.8:g.72110621G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4692C= MANE Select ENSP00000377233.3:n.509+4692C=
ENST00000334211.12:c.-305C= ENSP00000335506.8:n.-305C=
ENST00000359373.9:c.509+4692C= ENSP00000352332.5:n.509+4692C=
ENST00000393609.7:c.509+4692C= ENSP00000377233.3:n.509+4692C=
ENST00000426523.5:c.-305C= ENSP00000392264.1:n.-305C=
ENST00000429686.5:c.-305C= ENSP00000403127.1:n.-305C=
ENST00000465814.5:n.161C=
NM_001040118.2:c.509+4692C= NP_001035207.1:n.509+4692C=
NM_001135190.1:c.-305C= NP_001128662.1:n.-305C=
NM_015242.4:c.-305C= NP_056057.2:n.-305C=
NM_001369489.1:c.-305C= NP_001356418.1:n.-305C=
NR_161388.1:n.413C=
NM_001040118.3:c.509+4692C= MANE Select NP_001035207.1:n.509+4692C=
NM_001135190.2:c.-305C= NP_001128662.1:n.-305C=
NM_015242.5:c.-305C= NP_056057.2:n.-305C=