Canonical Allele Identifier: CA1982116875

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722171_72722173delinsGAA , CM000673.2:g.72722171_72722173delinsGAA	GRCh38
NC_000011.9:g.72433216_72433218delinsGAA , CM000673.1:g.72433216_72433218delinsGAA	GRCh37
NC_000011.8:g.72110864_72110866delinsGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4447_509+4449delinsTTC MANE Select	ENSP00000377233.3:n.509+4447_509+4449delinsTTC
ENST00000334211.12:c.-550_-548delinsTTC	ENSP00000335506.8:n.-550_-548delinsTTC
ENST00000359373.9:c.509+4447_509+4449delinsTTC	ENSP00000352332.5:n.509+4447_509+4449delinsTTC
ENST00000393609.7:c.509+4447_509+4449delinsTTC	ENSP00000377233.3:n.509+4447_509+4449delinsTTC
NM_001040118.2:c.509+4447_509+4449delinsTTC	NP_001035207.1:n.509+4447_509+4449delinsTTC
NM_001135190.1:c.-550_-548delinsTTC	NP_001128662.1:n.-550_-548delinsTTC
NM_015242.4:c.-550_-548delinsTTC	NP_056057.2:n.-550_-548delinsTTC
NM_001369489.1:c.-550_-548delinsTTC	NP_001356418.1:n.-550_-548delinsTTC
NR_161388.1:n.168_170delinsTTC
NM_001040118.3:c.509+4447_509+4449delinsTTC MANE Select	NP_001035207.1:n.509+4447_509+4449delinsTTC
NM_001135190.2:c.-550_-548delinsTTC	NP_001128662.1:n.-550_-548delinsTTC
NM_015242.5:c.-550_-548delinsTTC	NP_056057.2:n.-550_-548delinsTTC