Canonical Allele Identifier: CA679994432

Gene: ARAP1

Linked Data

• dbSNP Id: rs1200278592
• gnomAD v3: 11-72722202-TGTGA-T
• gnomAD v4: 11-72722202-TGTGA-T
• MyVariant Identifiers: chr11:g.72433248_72433251del (hg19) ; chr11:g.72722203_72722206del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722206_72722209del , CM000673.2:g.72722206_72722209del	GRCh38
NC_000011.9:g.72433251_72433254del , CM000673.1:g.72433251_72433254del	GRCh37
NC_000011.8:g.72110899_72110902del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4414_509+4417del MANE Select	ENSP00000377233.3:n.509+4414_509+4417del
ENST00000334211.12:c.-583_-580del	ENSP00000335506.8:n.-583_-580del
ENST00000359373.9:c.509+4414_509+4417del	ENSP00000352332.5:n.509+4414_509+4417del
ENST00000393609.7:c.509+4414_509+4417del	ENSP00000377233.3:n.509+4414_509+4417del
NM_001040118.2:c.509+4414_509+4417del	NP_001035207.1:n.509+4414_509+4417del
NM_001135190.1:c.-583_-580del	NP_001128662.1:n.-583_-580del
NM_015242.4:c.-583_-580del	NP_056057.2:n.-583_-580del
NM_001369489.1:c.-583_-580del	NP_001356418.1:n.-583_-580del
NR_161388.1:n.135_138del
NM_001040118.3:c.509+4414_509+4417del MANE Select	NP_001035207.1:n.509+4414_509+4417del
NM_001135190.2:c.-583_-580del	NP_001128662.1:n.-583_-580del
NM_015242.5:c.-583_-580del	NP_056057.2:n.-583_-580del