Canonical Allele Identifier: CA1982116874

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722170_72722171delinsAG , CM000673.2:g.72722170_72722171delinsAG	GRCh38
NC_000011.9:g.72433215_72433216delinsAG , CM000673.1:g.72433215_72433216delinsAG	GRCh37
NC_000011.8:g.72110863_72110864delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4449_509+4450delinsCT MANE Select	ENSP00000377233.3:n.509+4449_509+4450delinsCT
ENST00000334211.12:c.-548_-547delinsCT	ENSP00000335506.8:n.-548_-547delinsCT
ENST00000359373.9:c.509+4449_509+4450delinsCT	ENSP00000352332.5:n.509+4449_509+4450delinsCT
ENST00000393609.7:c.509+4449_509+4450delinsCT	ENSP00000377233.3:n.509+4449_509+4450delinsCT
NM_001040118.2:c.509+4449_509+4450delinsCT	NP_001035207.1:n.509+4449_509+4450delinsCT
NM_001135190.1:c.-548_-547delinsCT	NP_001128662.1:n.-548_-547delinsCT
NM_015242.4:c.-548_-547delinsCT	NP_056057.2:n.-548_-547delinsCT
NM_001369489.1:c.-548_-547delinsCT	NP_001356418.1:n.-548_-547delinsCT
NR_161388.1:n.170_171delinsCT
NM_001040118.3:c.509+4449_509+4450delinsCT MANE Select	NP_001035207.1:n.509+4449_509+4450delinsCT
NM_001135190.2:c.-548_-547delinsCT	NP_001128662.1:n.-548_-547delinsCT
NM_015242.5:c.-548_-547delinsCT	NP_056057.2:n.-548_-547delinsCT