Canonical Allele Identifier: CA939468585
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1835770281

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722151_72722154del , CM000673.2:g.72722151_72722154del GRCh38
NC_000011.9:g.72433196_72433199del , CM000673.1:g.72433196_72433199del GRCh37
NC_000011.8:g.72110844_72110847del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4468_509+4471del MANE Select ENSP00000377233.3:n.509+4468_509+4471del
ENST00000334211.12:c.-529_-526del ENSP00000335506.8:n.-529_-526del
ENST00000359373.9:c.509+4468_509+4471del ENSP00000352332.5:n.509+4468_509+4471del
ENST00000393609.7:c.509+4468_509+4471del ENSP00000377233.3:n.509+4468_509+4471del
NM_001040118.2:c.509+4468_509+4471del NP_001035207.1:n.509+4468_509+4471del
NM_001135190.1:c.-529_-526del NP_001128662.1:n.-529_-526del
NM_015242.4:c.-529_-526del NP_056057.2:n.-529_-526del
NM_001369489.1:c.-529_-526del NP_001356418.1:n.-529_-526del
NR_161388.1:n.189_192del
NM_001040118.3:c.509+4468_509+4471del MANE Select NP_001035207.1:n.509+4468_509+4471del
NM_001135190.2:c.-529_-526del NP_001128662.1:n.-529_-526del
NM_015242.5:c.-529_-526del NP_056057.2:n.-529_-526del