Canonical Allele Identifier: CA1982116893

Gene: ARAP1

Linked Data

• dbSNP Id: rs10675016
• gnomAD v4: 11-72722182-G-GGAGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722192_72722197dup , CM000673.2:g.72722192_72722197dup	GRCh38
NC_000011.9:g.72433237_72433242dup , CM000673.1:g.72433237_72433242dup	GRCh37
NC_000011.8:g.72110885_72110890dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4432_509+4437dup MANE Select	ENSP00000377233.3:n.509+4432_509+4437dup
ENST00000334211.12:c.-565_-560dup	ENSP00000335506.8:n.-565_-560dup
ENST00000359373.9:c.509+4432_509+4437dup	ENSP00000352332.5:n.509+4432_509+4437dup
ENST00000393609.7:c.509+4432_509+4437dup	ENSP00000377233.3:n.509+4432_509+4437dup
NM_001040118.2:c.509+4432_509+4437dup	NP_001035207.1:n.509+4432_509+4437dup
NM_001135190.1:c.-565_-560dup	NP_001128662.1:n.-565_-560dup
NM_015242.4:c.-565_-560dup	NP_056057.2:n.-565_-560dup
NM_001369489.1:c.-565_-560dup	NP_001356418.1:n.-565_-560dup
NR_161388.1:n.153_158dup
NM_001040118.3:c.509+4432_509+4437dup MANE Select	NP_001035207.1:n.509+4432_509+4437dup
NM_001135190.2:c.-565_-560dup	NP_001128662.1:n.-565_-560dup
NM_015242.5:c.-565_-560dup	NP_056057.2:n.-565_-560dup