Canonical Allele Identifier: CA679994339

Gene: ARAP1

Linked Data

• dbSNP Id: rs1376403486
• gnomAD v4: 11-72722100-CGT-C
• MyVariant Identifiers: chr11:g.72433146_72433147del (hg19) ; chr11:g.72722101_72722102del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722107_72722108del , CM000673.2:g.72722107_72722108del	GRCh38
NC_000011.9:g.72433152_72433153del , CM000673.1:g.72433152_72433153del	GRCh37
NC_000011.8:g.72110800_72110801del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4518_509+4519del MANE Select	ENSP00000377233.3:n.509+4518_509+4519del
ENST00000334211.12:c.-479_-478del	ENSP00000335506.8:n.-479_-478del
ENST00000359373.9:c.509+4518_509+4519del	ENSP00000352332.5:n.509+4518_509+4519del
ENST00000393609.7:c.509+4518_509+4519del	ENSP00000377233.3:n.509+4518_509+4519del
NM_001040118.2:c.509+4518_509+4519del	NP_001035207.1:n.509+4518_509+4519del
NM_001135190.1:c.-479_-478del	NP_001128662.1:n.-479_-478del
NM_015242.4:c.-479_-478del	NP_056057.2:n.-479_-478del
NM_001369489.1:c.-479_-478del	NP_001356418.1:n.-479_-478del
NR_161388.1:n.239_240del
NM_001040118.3:c.509+4518_509+4519del MANE Select	NP_001035207.1:n.509+4518_509+4519del
NM_001135190.2:c.-479_-478del	NP_001128662.1:n.-479_-478del
NM_015242.5:c.-479_-478del	NP_056057.2:n.-479_-478del