Canonical Allele Identifier: CA679994503

Gene: ARAP1

Linked Data

• dbSNP Id: rs1373963209
• MyVariant Identifiers: chr11:g.72433333_72433334del (hg19) ; chr11:g.72722288_72722289del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722291_72722292del , CM000673.2:g.72722291_72722292del	GRCh38
NC_000011.9:g.72433336_72433337del , CM000673.1:g.72433336_72433337del	GRCh37
NC_000011.8:g.72110984_72110985del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4331_509+4332del MANE Select	ENSP00000377233.3:n.509+4331_509+4332del
ENST00000334211.12:c.-666_-665del	ENSP00000335506.8:n.-666_-665del
ENST00000359373.9:c.509+4331_509+4332del	ENSP00000352332.5:n.509+4331_509+4332del
ENST00000393609.7:c.509+4331_509+4332del	ENSP00000377233.3:n.509+4331_509+4332del
NM_001040118.2:c.509+4331_509+4332del	NP_001035207.1:n.509+4331_509+4332del
NM_001135190.1:c.-666_-665del	NP_001128662.1:n.-666_-665del
NM_015242.4:c.-666_-665del	NP_056057.2:n.-666_-665del
NM_001369489.1:c.-666_-665del	NP_001356418.1:n.-666_-665del
NR_161388.1:n.52_53del
NM_001040118.3:c.509+4331_509+4332del MANE Select	NP_001035207.1:n.509+4331_509+4332del
NM_001135190.2:c.-666_-665del	NP_001128662.1:n.-666_-665del
NM_015242.5:c.-666_-665del	NP_056057.2:n.-666_-665del