Canonical Allele Identifier: CA224453160

Gene: ARAP1

Linked Data

• dbSNP Id: rs746406600
• gnomAD v2: 11-72433280-ATG-A
• gnomAD v3: 11-72722235-ATG-A
• gnomAD v4: 11-72722235-ATG-A
• MyVariant Identifiers: chr11:g.72433281_72433282del (hg19) ; chr11:g.72722236_72722237del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722245_72722246del , CM000673.2:g.72722245_72722246del	GRCh38
NC_000011.9:g.72433290_72433291del , CM000673.1:g.72433290_72433291del	GRCh37
NC_000011.8:g.72110938_72110939del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4383_509+4384del MANE Select	ENSP00000377233.3:n.509+4383_509+4384del
ENST00000334211.12:c.-614_-613del	ENSP00000335506.8:n.-614_-613del
ENST00000359373.9:c.509+4383_509+4384del	ENSP00000352332.5:n.509+4383_509+4384del
ENST00000393609.7:c.509+4383_509+4384del	ENSP00000377233.3:n.509+4383_509+4384del
NM_001040118.2:c.509+4383_509+4384del	NP_001035207.1:n.509+4383_509+4384del
NM_001135190.1:c.-614_-613del	NP_001128662.1:n.-614_-613del
NM_015242.4:c.-614_-613del	NP_056057.2:n.-614_-613del
NM_001369489.1:c.-614_-613del	NP_001356418.1:n.-614_-613del
NR_161388.1:n.104_105del
NM_001040118.3:c.509+4383_509+4384del MANE Select	NP_001035207.1:n.509+4383_509+4384del
NM_001135190.2:c.-614_-613del	NP_001128662.1:n.-614_-613del
NM_015242.5:c.-614_-613del	NP_056057.2:n.-614_-613del