Canonical Allele Identifier: CA2614979007

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722341-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722342_72722343del , CM000673.2:g.72722342_72722343del	GRCh38
NC_000011.9:g.72433387_72433388del , CM000673.1:g.72433387_72433388del	GRCh37
NC_000011.8:g.72111035_72111036del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4277_509+4278del MANE Select	ENSP00000377233.3:n.509+4277_509+4278del
ENST00000334211.12:c.-720_-719del	ENSP00000335506.8:n.-720_-719del
ENST00000359373.9:c.509+4277_509+4278del	ENSP00000352332.5:n.509+4277_509+4278del
ENST00000393609.7:c.509+4277_509+4278del	ENSP00000377233.3:n.509+4277_509+4278del
NM_001040118.2:c.509+4277_509+4278del	NP_001035207.1:n.509+4277_509+4278del
NM_001135190.1:c.-720_-719del	NP_001128662.1:n.-720_-719del
NM_015242.4:c.-720_-719del	NP_056057.2:n.-720_-719del
NM_001040118.3:c.509+4277_509+4278del MANE Select	NP_001035207.1:n.509+4277_509+4278del