Canonical Allele Identifier: CA2555768885

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722173_72722198dup , CM000673.2:g.72722173_72722198dup	GRCh38
NC_000011.9:g.72433218_72433243dup , CM000673.1:g.72433218_72433243dup	GRCh37
NC_000011.8:g.72110866_72110891dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4422_509+4447dup MANE Select	ENSP00000377233.3:n.509+4422_509+4447dup
ENST00000334211.12:c.-575_-550dup	ENSP00000335506.8:n.-575_-550dup
ENST00000359373.9:c.509+4422_509+4447dup	ENSP00000352332.5:n.509+4422_509+4447dup
ENST00000393609.7:c.509+4422_509+4447dup	ENSP00000377233.3:n.509+4422_509+4447dup
NM_001040118.2:c.509+4422_509+4447dup	NP_001035207.1:n.509+4422_509+4447dup
NM_001135190.1:c.-575_-550dup	NP_001128662.1:n.-575_-550dup
NM_015242.4:c.-575_-550dup	NP_056057.2:n.-575_-550dup
NM_001369489.1:c.-575_-550dup	NP_001356418.1:n.-575_-550dup
NR_161388.1:n.143_168dup
NM_001040118.3:c.509+4422_509+4447dup MANE Select	NP_001035207.1:n.509+4422_509+4447dup
NM_001135190.2:c.-575_-550dup	NP_001128662.1:n.-575_-550dup
NM_015242.5:c.-575_-550dup	NP_056057.2:n.-575_-550dup