Canonical Allele Identifier: CA2614978556

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722173-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722173_72722174insG , CM000673.2:g.72722173_72722174insG	GRCh38
NC_000011.9:g.72433218_72433219insG , CM000673.1:g.72433218_72433219insG	GRCh37
NC_000011.8:g.72110866_72110867insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4446_509+4447insC MANE Select	ENSP00000377233.3:n.509+4446_509+4447insC...
ENST00000334211.12:c.-551_-550insC	ENSP00000335506.8:n.-551_-550insC
ENST00000359373.9:c.509+4446_509+4447insC	ENSP00000352332.5:n.509+4446_509+4447insC...
ENST00000393609.7:c.509+4446_509+4447insC	ENSP00000377233.3:n.509+4446_509+4447insC...
NM_001040118.2:c.509+4446_509+4447insC	NP_001035207.1:n.509+4446_509+4447insC
NM_001135190.1:c.-551_-550insC	NP_001128662.1:n.-551_-550insC
NM_015242.4:c.-551_-550insC	NP_056057.2:n.-551_-550insC
NM_001369489.1:c.-551_-550insC	NP_001356418.1:n.-551_-550insC
NR_161388.1:n.167_168insC
NM_001040118.3:c.509+4446_509+4447insC MANE Select	NP_001035207.1:n.509+4446_509+4447insC
NM_001135190.2:c.-551_-550insC	NP_001128662.1:n.-551_-550insC
NM_015242.5:c.-551_-550insC	NP_056057.2:n.-551_-550insC