Canonical Allele Identifier: CA1982117055
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722468G= , CM000673.2:g.72722468G= GRCh38
NC_000011.9:g.72433513G= , CM000673.1:g.72433513G= GRCh37
NC_000011.8:g.72111161G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4152C= MANE Select ENSP00000377233.3:n.509+4152C=
ENST00000359373.9:c.509+4152C= ENSP00000352332.5:n.509+4152C=
ENST00000393609.7:c.509+4152C= ENSP00000377233.3:n.509+4152C=
NM_001040118.2:c.509+4152C= NP_001035207.1:n.509+4152C=
NM_001040118.3:c.509+4152C= MANE Select NP_001035207.1:n.509+4152C=