Canonical Allele Identifier: CA224453141

Gene: ARAP1

Linked Data

• dbSNP Id: rs10675016
• gnomAD v2: 11-72433227-GGAGA-G
• gnomAD v3: 11-72722182-GGAGA-G
• gnomAD v4: 11-72722182-GGAGA-G
• MyVariant Identifiers: chr11:g.72433228_72433231del (hg19) ; chr11:g.72722183_72722186del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722194_72722197del , CM000673.2:g.72722194_72722197del	GRCh38
NC_000011.9:g.72433239_72433242del , CM000673.1:g.72433239_72433242del	GRCh37
NC_000011.8:g.72110887_72110890del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4434_509+4437del MANE Select	ENSP00000377233.3:n.509+4434_509+4437del
ENST00000334211.12:c.-563_-560del	ENSP00000335506.8:n.-563_-560del
ENST00000359373.9:c.509+4434_509+4437del	ENSP00000352332.5:n.509+4434_509+4437del
ENST00000393609.7:c.509+4434_509+4437del	ENSP00000377233.3:n.509+4434_509+4437del
NM_001040118.2:c.509+4434_509+4437del	NP_001035207.1:n.509+4434_509+4437del
NM_001135190.1:c.-563_-560del	NP_001128662.1:n.-563_-560del
NM_015242.4:c.-563_-560del	NP_056057.2:n.-563_-560del
NM_001369489.1:c.-563_-560del	NP_001356418.1:n.-563_-560del
NR_161388.1:n.155_158del
NM_001040118.3:c.509+4434_509+4437del MANE Select	NP_001035207.1:n.509+4434_509+4437del
NM_001135190.2:c.-563_-560del	NP_001128662.1:n.-563_-560del
NM_015242.5:c.-563_-560del	NP_056057.2:n.-563_-560del