Canonical Allele Identifier: CA600098584

Gene: ARAP1

Linked Data

• dbSNP Id: rs1477158617
• gnomAD v2: 11-72433217-AAAGAC-A
• gnomAD v4: 11-72722172-AAAGAC-A
• MyVariant Identifiers: chr11:g.72433218_72433222del (hg19) ; chr11:g.72722173_72722177del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722174_72722178del , CM000673.2:g.72722174_72722178del	GRCh38
NC_000011.9:g.72433219_72433223del , CM000673.1:g.72433219_72433223del	GRCh37
NC_000011.8:g.72110867_72110871del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4443_509+4447del MANE Select	ENSP00000377233.3:n.509+4443_509+4447del
ENST00000334211.12:c.-554_-550del	ENSP00000335506.8:n.-554_-550del
ENST00000359373.9:c.509+4443_509+4447del	ENSP00000352332.5:n.509+4443_509+4447del
ENST00000393609.7:c.509+4443_509+4447del	ENSP00000377233.3:n.509+4443_509+4447del
NM_001040118.2:c.509+4443_509+4447del	NP_001035207.1:n.509+4443_509+4447del
NM_001135190.1:c.-554_-550del	NP_001128662.1:n.-554_-550del
NM_015242.4:c.-554_-550del	NP_056057.2:n.-554_-550del
NM_001369489.1:c.-554_-550del	NP_001356418.1:n.-554_-550del
NR_161388.1:n.164_168del
NM_001040118.3:c.509+4443_509+4447del MANE Select	NP_001035207.1:n.509+4443_509+4447del
NM_001135190.2:c.-554_-550del	NP_001128662.1:n.-554_-550del
NM_015242.5:c.-554_-550del	NP_056057.2:n.-554_-550del