Canonical Allele Identifier: CA1982116933

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722235_72722237delinsATG , CM000673.2:g.72722235_72722237delinsATG	GRCh38
NC_000011.9:g.72433280_72433282delinsATG , CM000673.1:g.72433280_72433282delinsATG	GRCh37
NC_000011.8:g.72110928_72110930delinsATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4383_509+4385delinsCAT MANE Select	ENSP00000377233.3:n.509+4383_509+4385delinsCAT
ENST00000334211.12:c.-614_-612delinsCAT	ENSP00000335506.8:n.-614_-612delinsCAT
ENST00000359373.9:c.509+4383_509+4385delinsCAT	ENSP00000352332.5:n.509+4383_509+4385delinsCAT
ENST00000393609.7:c.509+4383_509+4385delinsCAT	ENSP00000377233.3:n.509+4383_509+4385delinsCAT
NM_001040118.2:c.509+4383_509+4385delinsCAT	NP_001035207.1:n.509+4383_509+4385delinsCAT
NM_001135190.1:c.-614_-612delinsCAT	NP_001128662.1:n.-614_-612delinsCAT
NM_015242.4:c.-614_-612delinsCAT	NP_056057.2:n.-614_-612delinsCAT
NM_001369489.1:c.-614_-612delinsCAT	NP_001356418.1:n.-614_-612delinsCAT
NR_161388.1:n.104_106delinsCAT
NM_001040118.3:c.509+4383_509+4385delinsCAT MANE Select	NP_001035207.1:n.509+4383_509+4385delinsCAT
NM_001135190.2:c.-614_-612delinsCAT	NP_001128662.1:n.-614_-612delinsCAT
NM_015242.5:c.-614_-612delinsCAT	NP_056057.2:n.-614_-612delinsCAT