Canonical Allele Identifier: CA1982116984

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722319_72722321delinsAAC , CM000673.2:g.72722319_72722321delinsAAC	GRCh38
NC_000011.9:g.72433364_72433366delinsAAC , CM000673.1:g.72433364_72433366delinsAAC	GRCh37
NC_000011.8:g.72111012_72111014delinsAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4299_509+4301delinsGTT MANE Select	ENSP00000377233.3:n.509+4299_509+4301delinsGTT
ENST00000334211.12:c.-698_-696delinsGTT	ENSP00000335506.8:n.-698_-696delinsGTT
ENST00000359373.9:c.509+4299_509+4301delinsGTT	ENSP00000352332.5:n.509+4299_509+4301delinsGTT
ENST00000393609.7:c.509+4299_509+4301delinsGTT	ENSP00000377233.3:n.509+4299_509+4301delinsGTT
NM_001040118.2:c.509+4299_509+4301delinsGTT	NP_001035207.1:n.509+4299_509+4301delinsGTT
NM_001135190.1:c.-698_-696delinsGTT	NP_001128662.1:n.-698_-696delinsGTT
NM_015242.4:c.-698_-696delinsGTT	NP_056057.2:n.-698_-696delinsGTT
NM_001369489.1:c.-698_-696delinsGTT	NP_001356418.1:n.-698_-696delinsGTT
NR_161388.1:n.20_22delinsGTT
NM_001040118.3:c.509+4299_509+4301delinsGTT MANE Select	NP_001035207.1:n.509+4299_509+4301delinsGTT
NM_001135190.2:c.-698_-696delinsGTT	NP_001128662.1:n.-698_-696delinsGTT
NM_015242.5:c.-698_-696delinsGTT	NP_056057.2:n.-698_-696delinsGTT