Canonical Allele Identifier: CA679994301

Gene: ARAP1

Linked Data

• dbSNP Id: rs1286809274
• gnomAD v3: 11-72722052-CA-C
• gnomAD v4: 11-72722052-CA-C
• MyVariant Identifiers: chr11:g.72433098del (hg19) ; chr11:g.72722053del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722053del , CM000673.2:g.72722053del	GRCh38
NC_000011.9:g.72433098del , CM000673.1:g.72433098del	GRCh37
NC_000011.8:g.72110746del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4567del MANE Select	ENSP00000377233.3:n.509+4567del
ENST00000334211.12:c.-430del	ENSP00000335506.8:n.-430del
ENST00000359373.9:c.509+4567del	ENSP00000352332.5:n.509+4567del
ENST00000393609.7:c.509+4567del	ENSP00000377233.3:n.509+4567del
ENST00000465814.5:n.36del
NM_001040118.2:c.509+4567del	NP_001035207.1:n.509+4567del
NM_001135190.1:c.-430del	NP_001128662.1:n.-430del
NM_015242.4:c.-430del	NP_056057.2:n.-430del
NM_001369489.1:c.-430del	NP_001356418.1:n.-430del
NR_161388.1:n.288del
NM_001040118.3:c.509+4567del MANE Select	NP_001035207.1:n.509+4567del
NM_001135190.2:c.-430del	NP_001128662.1:n.-430del
NM_015242.5:c.-430del	NP_056057.2:n.-430del