Canonical Allele Identifier: CA2614978769

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722216-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722219_72722220del , CM000673.2:g.72722219_72722220del	GRCh38
NC_000011.9:g.72433264_72433265del , CM000673.1:g.72433264_72433265del	GRCh37
NC_000011.8:g.72110912_72110913del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4402_509+4403del MANE Select	ENSP00000377233.3:n.509+4402_509+4403del
ENST00000334211.12:c.-595_-594del	ENSP00000335506.8:n.-595_-594del
ENST00000359373.9:c.509+4402_509+4403del	ENSP00000352332.5:n.509+4402_509+4403del
ENST00000393609.7:c.509+4402_509+4403del	ENSP00000377233.3:n.509+4402_509+4403del
NM_001040118.2:c.509+4402_509+4403del	NP_001035207.1:n.509+4402_509+4403del
NM_001135190.1:c.-595_-594del	NP_001128662.1:n.-595_-594del
NM_015242.4:c.-595_-594del	NP_056057.2:n.-595_-594del
NM_001369489.1:c.-595_-594del	NP_001356418.1:n.-595_-594del
NR_161388.1:n.123_124del
NM_001040118.3:c.509+4402_509+4403del MANE Select	NP_001035207.1:n.509+4402_509+4403del
NM_001135190.2:c.-595_-594del	NP_001128662.1:n.-595_-594del
NM_015242.5:c.-595_-594del	NP_056057.2:n.-595_-594del