Canonical Allele Identifier: CA1982116865

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722165_72722173delinsGAGAGAGAA , CM000673.2:g.72722165_72722173delinsGAGAGAGAA	GRCh38
NC_000011.9:g.72433210_72433218delinsGAGAGAGAA , CM000673.1:g.72433210_72433218delinsGAGAGAGAA	GRCh37
NC_000011.8:g.72110858_72110866delinsGAGAGAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4447_509+4455delinsTTCTCTCTC MANE Select	ENSP00000377233.3:n.509+4447_509+4455delinsTTCTCTCTC
ENST00000334211.12:c.-550_-542delinsTTCTCTCTC	ENSP00000335506.8:n.-550_-542delinsTTCTCTCTC
ENST00000359373.9:c.509+4447_509+4455delinsTTCTCTCTC	ENSP00000352332.5:n.509+4447_509+4455delinsTTCTCTCTC
ENST00000393609.7:c.509+4447_509+4455delinsTTCTCTCTC	ENSP00000377233.3:n.509+4447_509+4455delinsTTCTCTCTC
NM_001040118.2:c.509+4447_509+4455delinsTTCTCTCTC	NP_001035207.1:n.509+4447_509+4455delinsTTCTCTCTC
NM_001135190.1:c.-550_-542delinsTTCTCTCTC	NP_001128662.1:n.-550_-542delinsTTCTCTCTC
NM_015242.4:c.-550_-542delinsTTCTCTCTC	NP_056057.2:n.-550_-542delinsTTCTCTCTC
NM_001369489.1:c.-550_-542delinsTTCTCTCTC	NP_001356418.1:n.-550_-542delinsTTCTCTCTC
NR_161388.1:n.168_176delinsTTCTCTCTC
NM_001040118.3:c.509+4447_509+4455delinsTTCTCTCTC MANE Select	NP_001035207.1:n.509+4447_509+4455delinsTTCTCTCTC
NM_001135190.2:c.-550_-542delinsTTCTCTCTC	NP_001128662.1:n.-550_-542delinsTTCTCTCTC
NM_015242.5:c.-550_-542delinsTTCTCTCTC	NP_056057.2:n.-550_-542delinsTTCTCTCTC