Canonical Allele Identifier: CA224453118

Gene: ARAP1

Linked Data

• dbSNP Id: rs200194585
• gnomAD v4: 11-72722149-GAC-G
• MyVariant Identifiers: chr11:g.72433195_72433196del (hg19) ; chr11:g.72722150_72722151del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722151_72722152del , CM000673.2:g.72722151_72722152del	GRCh38
NC_000011.9:g.72433196_72433197del , CM000673.1:g.72433196_72433197del	GRCh37
NC_000011.8:g.72110844_72110845del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4469_509+4470del MANE Select	ENSP00000377233.3:n.509+4469_509+4470del
ENST00000334211.12:c.-528_-527del	ENSP00000335506.8:n.-528_-527del
ENST00000359373.9:c.509+4469_509+4470del	ENSP00000352332.5:n.509+4469_509+4470del
ENST00000393609.7:c.509+4469_509+4470del	ENSP00000377233.3:n.509+4469_509+4470del
NM_001040118.2:c.509+4469_509+4470del	NP_001035207.1:n.509+4469_509+4470del
NM_001135190.1:c.-528_-527del	NP_001128662.1:n.-528_-527del
NM_015242.4:c.-528_-527del	NP_056057.2:n.-528_-527del
NM_001369489.1:c.-528_-527del	NP_001356418.1:n.-528_-527del
NR_161388.1:n.190_191del
NM_001040118.3:c.509+4469_509+4470del MANE Select	NP_001035207.1:n.509+4469_509+4470del
NM_001135190.2:c.-528_-527del	NP_001128662.1:n.-528_-527del
NM_015242.5:c.-528_-527del	NP_056057.2:n.-528_-527del