Canonical Allele Identifier: CA1982116790
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722014C= , CM000673.2:g.72722014C= GRCh38
NC_000011.9:g.72433059C= , CM000673.1:g.72433059C= GRCh37
NC_000011.8:g.72110707C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4606G= MANE Select ENSP00000377233.3:n.509+4606G=
ENST00000334211.12:c.-391G= ENSP00000335506.8:n.-391G=
ENST00000359373.9:c.509+4606G= ENSP00000352332.5:n.509+4606G=
ENST00000393609.7:c.509+4606G= ENSP00000377233.3:n.509+4606G=
ENST00000426523.5:c.-391G= ENSP00000392264.1:n.-391G=
ENST00000429686.5:c.-391G= ENSP00000403127.1:n.-391G=
ENST00000465814.5:n.75G=
NM_001040118.2:c.509+4606G= NP_001035207.1:n.509+4606G=
NM_001135190.1:c.-391G= NP_001128662.1:n.-391G=
NM_015242.4:c.-391G= NP_056057.2:n.-391G=
NM_001369489.1:c.-391G= NP_001356418.1:n.-391G=
NR_161388.1:n.327G=
NM_001040118.3:c.509+4606G= MANE Select NP_001035207.1:n.509+4606G=
NM_001135190.2:c.-391G= NP_001128662.1:n.-391G=
NM_015242.5:c.-391G= NP_056057.2:n.-391G=