Canonical Allele Identifier: CA1982116900

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722193_72722194delinsGA , CM000673.2:g.72722193_72722194delinsGA	GRCh38
NC_000011.9:g.72433238_72433239delinsGA , CM000673.1:g.72433238_72433239delinsGA	GRCh37
NC_000011.8:g.72110886_72110887delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4426_509+4427delinsTC MANE Select	ENSP00000377233.3:n.509+4426_509+4427delinsTC
ENST00000334211.12:c.-571_-570delinsTC	ENSP00000335506.8:n.-571_-570delinsTC
ENST00000359373.9:c.509+4426_509+4427delinsTC	ENSP00000352332.5:n.509+4426_509+4427delinsTC
ENST00000393609.7:c.509+4426_509+4427delinsTC	ENSP00000377233.3:n.509+4426_509+4427delinsTC
NM_001040118.2:c.509+4426_509+4427delinsTC	NP_001035207.1:n.509+4426_509+4427delinsTC
NM_001135190.1:c.-571_-570delinsTC	NP_001128662.1:n.-571_-570delinsTC
NM_015242.4:c.-571_-570delinsTC	NP_056057.2:n.-571_-570delinsTC
NM_001369489.1:c.-571_-570delinsTC	NP_001356418.1:n.-571_-570delinsTC
NR_161388.1:n.147_148delinsTC
NM_001040118.3:c.509+4426_509+4427delinsTC MANE Select	NP_001035207.1:n.509+4426_509+4427delinsTC
NM_001135190.2:c.-571_-570delinsTC	NP_001128662.1:n.-571_-570delinsTC
NM_015242.5:c.-571_-570delinsTC	NP_056057.2:n.-571_-570delinsTC