Canonical Allele Identifier: CA2614978514

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722166-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722167_72722168insGG , CM000673.2:g.72722167_72722168insGG	GRCh38
NC_000011.9:g.72433212_72433213insGG , CM000673.1:g.72433212_72433213insGG	GRCh37
NC_000011.8:g.72110860_72110861insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4453_509+4454insCC MANE Select	ENSP00000377233.3:n.509+4453_509+4454insCC
ENST00000334211.12:c.-544_-543insCC	ENSP00000335506.8:n.-544_-543insCC
ENST00000359373.9:c.509+4453_509+4454insCC	ENSP00000352332.5:n.509+4453_509+4454insCC
ENST00000393609.7:c.509+4453_509+4454insCC	ENSP00000377233.3:n.509+4453_509+4454insCC
NM_001040118.2:c.509+4453_509+4454insCC	NP_001035207.1:n.509+4453_509+4454insCC
NM_001135190.1:c.-544_-543insCC	NP_001128662.1:n.-544_-543insCC
NM_015242.4:c.-544_-543insCC	NP_056057.2:n.-544_-543insCC
NM_001369489.1:c.-544_-543insCC	NP_001356418.1:n.-544_-543insCC
NR_161388.1:n.174_175insCC
NM_001040118.3:c.509+4453_509+4454insCC MANE Select	NP_001035207.1:n.509+4453_509+4454insCC
NM_001135190.2:c.-544_-543insCC	NP_001128662.1:n.-544_-543insCC
NM_015242.5:c.-544_-543insCC	NP_056057.2:n.-544_-543insCC