Canonical Allele Identifier: CA2614978512

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722166-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722167del , CM000673.2:g.72722167del	GRCh38
NC_000011.9:g.72433212del , CM000673.1:g.72433212del	GRCh37
NC_000011.8:g.72110860del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4453del MANE Select	ENSP00000377233.3:n.509+4453del
ENST00000334211.12:c.-544del	ENSP00000335506.8:n.-544del
ENST00000359373.9:c.509+4453del	ENSP00000352332.5:n.509+4453del
ENST00000393609.7:c.509+4453del	ENSP00000377233.3:n.509+4453del
NM_001040118.2:c.509+4453del	NP_001035207.1:n.509+4453del
NM_001135190.1:c.-544del	NP_001128662.1:n.-544del
NM_015242.4:c.-544del	NP_056057.2:n.-544del
NM_001369489.1:c.-544del	NP_001356418.1:n.-544del
NR_161388.1:n.174del
NM_001040118.3:c.509+4453del MANE Select	NP_001035207.1:n.509+4453del
NM_001135190.2:c.-544del	NP_001128662.1:n.-544del
NM_015242.5:c.-544del	NP_056057.2:n.-544del