Canonical Allele Identifier: CA2599048245
Gene: ARAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722171_72722177del , CM000673.2:g.72722171_72722177del GRCh38
NC_000011.9:g.72433216_72433222del , CM000673.1:g.72433216_72433222del GRCh37
NC_000011.8:g.72110864_72110870del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4443_509+4449del MANE Select ENSP00000377233.3:n.509+4443_509+4449del
ENST00000334211.12:c.-554_-548del ENSP00000335506.8:n.-554_-548del
ENST00000359373.9:c.509+4443_509+4449del ENSP00000352332.5:n.509+4443_509+4449del
ENST00000393609.7:c.509+4443_509+4449del ENSP00000377233.3:n.509+4443_509+4449del
NM_001040118.2:c.509+4443_509+4449del NP_001035207.1:n.509+4443_509+4449del
NM_001135190.1:c.-554_-548del NP_001128662.1:n.-554_-548del
NM_015242.4:c.-554_-548del NP_056057.2:n.-554_-548del
NM_001369489.1:c.-554_-548del NP_001356418.1:n.-554_-548del
NR_161388.1:n.164_170del
NM_001040118.3:c.509+4443_509+4449del MANE Select NP_001035207.1:n.509+4443_509+4449del
NM_001135190.2:c.-554_-548del NP_001128662.1:n.-554_-548del
NM_015242.5:c.-554_-548del NP_056057.2:n.-554_-548del