Canonical Allele Identifier: CA1982116859

Gene: ARAP1

Linked Data

• dbSNP Id: rs1785139965
• gnomAD v4: 11-72722158-AGAGAGAGAGAGAGAAAGACAGAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722173_72722196del , CM000673.2:g.72722173_72722196del	GRCh38
NC_000011.9:g.72433218_72433241del , CM000673.1:g.72433218_72433241del	GRCh37
NC_000011.8:g.72110866_72110889del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4438_509+4461del MANE Select	ENSP00000377233.3:n.509+4438_509+4461del
ENST00000334211.12:c.-559_-536del	ENSP00000335506.8:n.-559_-536del
ENST00000359373.9:c.509+4438_509+4461del	ENSP00000352332.5:n.509+4438_509+4461del
ENST00000393609.7:c.509+4438_509+4461del	ENSP00000377233.3:n.509+4438_509+4461del
NM_001040118.2:c.509+4438_509+4461del	NP_001035207.1:n.509+4438_509+4461del
NM_001135190.1:c.-559_-536del	NP_001128662.1:n.-559_-536del
NM_015242.4:c.-559_-536del	NP_056057.2:n.-559_-536del
NM_001369489.1:c.-559_-536del	NP_001356418.1:n.-559_-536del
NR_161388.1:n.159_182del
NM_001040118.3:c.509+4438_509+4461del MANE Select	NP_001035207.1:n.509+4438_509+4461del
NM_001135190.2:c.-559_-536del	NP_001128662.1:n.-559_-536del
NM_015242.5:c.-559_-536del	NP_056057.2:n.-559_-536del