Canonical Allele Identifier: CA1982117035
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722407_72722408delinsAC , CM000673.2:g.72722407_72722408delinsAC GRCh38
NC_000011.9:g.72433452_72433453delinsAC , CM000673.1:g.72433452_72433453delinsAC GRCh37
NC_000011.8:g.72111100_72111101delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4212_509+4213delinsGT MANE Select ENSP00000377233.3:n.509+4212_509+4213delinsGT
ENST00000359373.9:c.509+4212_509+4213delinsGT ENSP00000352332.5:n.509+4212_509+4213delinsGT
ENST00000393609.7:c.509+4212_509+4213delinsGT ENSP00000377233.3:n.509+4212_509+4213delinsGT
NM_001040118.2:c.509+4212_509+4213delinsGT NP_001035207.1:n.509+4212_509+4213delinsGT
NM_001040118.3:c.509+4212_509+4213delinsGT MANE Select NP_001035207.1:n.509+4212_509+4213delinsGT