Canonical Allele Identifier: CA2792664005

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722226_72722228del , CM000673.2:g.72722226_72722228del	GRCh38
NC_000011.9:g.72433271_72433273del , CM000673.1:g.72433271_72433273del	GRCh37
NC_000011.8:g.72110919_72110921del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4392_509+4394del MANE Select	ENSP00000377233.3:n.509+4392_509+4394del
ENST00000334211.12:c.-605_-603del	ENSP00000335506.8:n.-605_-603del
ENST00000359373.9:c.509+4392_509+4394del	ENSP00000352332.5:n.509+4392_509+4394del
ENST00000393609.7:c.509+4392_509+4394del	ENSP00000377233.3:n.509+4392_509+4394del
NM_001040118.2:c.509+4392_509+4394del	NP_001035207.1:n.509+4392_509+4394del
NM_001135190.1:c.-605_-603del	NP_001128662.1:n.-605_-603del
NM_015242.4:c.-605_-603del	NP_056057.2:n.-605_-603del
NM_001369489.1:c.-605_-603del	NP_001356418.1:n.-605_-603del
NR_161388.1:n.113_115del
NM_001040118.3:c.509+4392_509+4394del MANE Select	NP_001035207.1:n.509+4392_509+4394del
NM_001135190.2:c.-605_-603del	NP_001128662.1:n.-605_-603del
NM_015242.5:c.-605_-603del	NP_056057.2:n.-605_-603del