Canonical Allele Identifier: CA1982116920

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722219_72722221delinsCTG , CM000673.2:g.72722219_72722221delinsCTG	GRCh38
NC_000011.9:g.72433264_72433266delinsCTG , CM000673.1:g.72433264_72433266delinsCTG	GRCh37
NC_000011.8:g.72110912_72110914delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4399_509+4401delinsCAG MANE Select	ENSP00000377233.3:n.509+4399_509+4401delinsCAG
ENST00000334211.12:c.-598_-596delinsCAG	ENSP00000335506.8:n.-598_-596delinsCAG
ENST00000359373.9:c.509+4399_509+4401delinsCAG	ENSP00000352332.5:n.509+4399_509+4401delinsCAG
ENST00000393609.7:c.509+4399_509+4401delinsCAG	ENSP00000377233.3:n.509+4399_509+4401delinsCAG
NM_001040118.2:c.509+4399_509+4401delinsCAG	NP_001035207.1:n.509+4399_509+4401delinsCAG
NM_001135190.1:c.-598_-596delinsCAG	NP_001128662.1:n.-598_-596delinsCAG
NM_015242.4:c.-598_-596delinsCAG	NP_056057.2:n.-598_-596delinsCAG
NM_001369489.1:c.-598_-596delinsCAG	NP_001356418.1:n.-598_-596delinsCAG
NR_161388.1:n.120_122delinsCAG
NM_001040118.3:c.509+4399_509+4401delinsCAG MANE Select	NP_001035207.1:n.509+4399_509+4401delinsCAG
NM_001135190.2:c.-598_-596delinsCAG	NP_001128662.1:n.-598_-596delinsCAG
NM_015242.5:c.-598_-596delinsCAG	NP_056057.2:n.-598_-596delinsCAG