Canonical Allele Identifier: CA1982116876

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722172_72722177delinsAAAGAC , CM000673.2:g.72722172_72722177delinsAAAGAC	GRCh38
NC_000011.9:g.72433217_72433222delinsAAAGAC , CM000673.1:g.72433217_72433222delinsAAAGAC	GRCh37
NC_000011.8:g.72110865_72110870delinsAAAGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4443_509+4448delinsGTCTTT MANE Select	ENSP00000377233.3:n.509+4443_509+4448delinsGTCTTT
ENST00000334211.12:c.-554_-549delinsGTCTTT	ENSP00000335506.8:n.-554_-549delinsGTCTTT
ENST00000359373.9:c.509+4443_509+4448delinsGTCTTT	ENSP00000352332.5:n.509+4443_509+4448delinsGTCTTT
ENST00000393609.7:c.509+4443_509+4448delinsGTCTTT	ENSP00000377233.3:n.509+4443_509+4448delinsGTCTTT
NM_001040118.2:c.509+4443_509+4448delinsGTCTTT	NP_001035207.1:n.509+4443_509+4448delinsGTCTTT
NM_001135190.1:c.-554_-549delinsGTCTTT	NP_001128662.1:n.-554_-549delinsGTCTTT
NM_015242.4:c.-554_-549delinsGTCTTT	NP_056057.2:n.-554_-549delinsGTCTTT
NM_001369489.1:c.-554_-549delinsGTCTTT	NP_001356418.1:n.-554_-549delinsGTCTTT
NR_161388.1:n.164_169delinsGTCTTT
NM_001040118.3:c.509+4443_509+4448delinsGTCTTT MANE Select	NP_001035207.1:n.509+4443_509+4448delinsGTCTTT
NM_001135190.2:c.-554_-549delinsGTCTTT	NP_001128662.1:n.-554_-549delinsGTCTTT
NM_015242.5:c.-554_-549delinsGTCTTT	NP_056057.2:n.-554_-549delinsGTCTTT