Canonical Allele Identifier: CA2555423358

Gene: ARAP1

Linked Data

• dbSNP Id: rs2135565134
• gnomAD v3: 11-72722151-C-CAGAGAGAGAGAGAGAGAGAAAGACAGAGGG
• gnomAD v4: 11-72722151-C-CAGAGAGAGAGAGAGAGAGAAAGACAGAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722170_72722171insAAGACAGAGGGAGAGAGAGAGAGAGAGAGA , CM000673.2:g.72722170_72722171insAAGACAGAGGGAGAGAGAGAGAGAGAGAGA	GRCh38
NC_000011.9:g.72433215_72433216insAAGACAGAGGGAGAGAGAGAGAGAGAGAGA , CM000673.1:g.72433215_72433216insAAGACAGAGGGAGAGAGAGAGAGAGAGAGA	GRCh37
NC_000011.8:g.72110863_72110864insAAGACAGAGGGAGAGAGAGAGAGAGAGAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT MANE Select	ENSP00000377233.3:n.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTC...
ENST00000334211.12:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	ENSP00000335506.8:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTC...
ENST00000359373.9:c.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	ENSP00000352332.5:n.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTC...
ENST00000393609.7:c.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	ENSP00000377233.3:n.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTC...
NM_001040118.2:c.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_001035207.1:n.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCT...
NM_001135190.1:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_001128662.1:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT
NM_015242.4:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_056057.2:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT
NM_001369489.1:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_001356418.1:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT
NR_161388.1:n.189_190insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT
NM_001040118.3:c.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT MANE Select	NP_001035207.1:n.509+4468_509+4469insCCCTCTGTCTTTCTCTCTCTCTCT...
NM_001135190.2:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_001128662.1:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT
NM_015242.5:c.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT	NP_056057.2:n.-529_-528insCCCTCTGTCTTTCTCTCTCTCTCTCTCTCT