Canonical Allele Identifier: CA1982116863

Gene: ARAP1

Linked Data

• dbSNP Id: rs1857541138
• gnomAD v4: 11-72722162-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722163_72722164insGG , CM000673.2:g.72722163_72722164insGG	GRCh38
NC_000011.9:g.72433208_72433209insGG , CM000673.1:g.72433208_72433209insGG	GRCh37
NC_000011.8:g.72110856_72110857insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4457_509+4458insCC MANE Select	ENSP00000377233.3:n.509+4457_509+4458insCC
ENST00000334211.12:c.-540_-539insCC	ENSP00000335506.8:n.-540_-539insCC
ENST00000359373.9:c.509+4457_509+4458insCC	ENSP00000352332.5:n.509+4457_509+4458insCC
ENST00000393609.7:c.509+4457_509+4458insCC	ENSP00000377233.3:n.509+4457_509+4458insCC
NM_001040118.2:c.509+4457_509+4458insCC	NP_001035207.1:n.509+4457_509+4458insCC
NM_001135190.1:c.-540_-539insCC	NP_001128662.1:n.-540_-539insCC
NM_015242.4:c.-540_-539insCC	NP_056057.2:n.-540_-539insCC
NM_001369489.1:c.-540_-539insCC	NP_001356418.1:n.-540_-539insCC
NR_161388.1:n.178_179insCC
NM_001040118.3:c.509+4457_509+4458insCC MANE Select	NP_001035207.1:n.509+4457_509+4458insCC
NM_001135190.2:c.-540_-539insCC	NP_001128662.1:n.-540_-539insCC
NM_015242.5:c.-540_-539insCC	NP_056057.2:n.-540_-539insCC