Canonical Allele Identifier: CA939468607

Gene: ARAP1

Linked Data

• dbSNP Id: rs1857540068
• gnomAD v3: 11-72722152-A-AGAGAGAGAGAGAGAGAGAGAAAGACAGAGG
• gnomAD v4: 11-72722152-A-AGAGAGAGAGAGAGAGAGAGAAAGACAGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722168_72722197dup , CM000673.2:g.72722168_72722197dup	GRCh38
NC_000011.9:g.72433213_72433242dup , CM000673.1:g.72433213_72433242dup	GRCh37
NC_000011.8:g.72110861_72110890dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4438_509+4467dup MANE Select	ENSP00000377233.3:n.509+4438_509+4467dup
ENST00000334211.12:c.-559_-530dup	ENSP00000335506.8:n.-559_-530dup
ENST00000359373.9:c.509+4438_509+4467dup	ENSP00000352332.5:n.509+4438_509+4467dup
ENST00000393609.7:c.509+4438_509+4467dup	ENSP00000377233.3:n.509+4438_509+4467dup
NM_001040118.2:c.509+4438_509+4467dup	NP_001035207.1:n.509+4438_509+4467dup
NM_001135190.1:c.-559_-530dup	NP_001128662.1:n.-559_-530dup
NM_015242.4:c.-559_-530dup	NP_056057.2:n.-559_-530dup
NM_001369489.1:c.-559_-530dup	NP_001356418.1:n.-559_-530dup
NR_161388.1:n.159_188dup
NM_001040118.3:c.509+4438_509+4467dup MANE Select	NP_001035207.1:n.509+4438_509+4467dup
NM_001135190.2:c.-559_-530dup	NP_001128662.1:n.-559_-530dup
NM_015242.5:c.-559_-530dup	NP_056057.2:n.-559_-530dup