Canonical Allele Identifier: CA2614978732

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722204-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722206_72722207dup , CM000673.2:g.72722206_72722207dup	GRCh38
NC_000011.9:g.72433251_72433252dup , CM000673.1:g.72433251_72433252dup	GRCh37
NC_000011.8:g.72110899_72110900dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4414_509+4415dup MANE Select	ENSP00000377233.3:n.509+4414_509+4415dup
ENST00000334211.12:c.-583_-582dup	ENSP00000335506.8:n.-583_-582dup
ENST00000359373.9:c.509+4414_509+4415dup	ENSP00000352332.5:n.509+4414_509+4415dup
ENST00000393609.7:c.509+4414_509+4415dup	ENSP00000377233.3:n.509+4414_509+4415dup
NM_001040118.2:c.509+4414_509+4415dup	NP_001035207.1:n.509+4414_509+4415dup
NM_001135190.1:c.-583_-582dup	NP_001128662.1:n.-583_-582dup
NM_015242.4:c.-583_-582dup	NP_056057.2:n.-583_-582dup
NM_001369489.1:c.-583_-582dup	NP_001356418.1:n.-583_-582dup
NR_161388.1:n.135_136dup
NM_001040118.3:c.509+4414_509+4415dup MANE Select	NP_001035207.1:n.509+4414_509+4415dup
NM_001135190.2:c.-583_-582dup	NP_001128662.1:n.-583_-582dup
NM_015242.5:c.-583_-582dup	NP_056057.2:n.-583_-582dup