Canonical Allele Identifier: CA2574916178

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722182_72722183dup , CM000673.2:g.72722182_72722183dup	GRCh38
NC_000011.9:g.72433227_72433228dup , CM000673.1:g.72433227_72433228dup	GRCh37
NC_000011.8:g.72110875_72110876dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4438_509+4439dup MANE Select	ENSP00000377233.3:n.509+4438_509+4439dup
ENST00000334211.12:c.-559_-558dup	ENSP00000335506.8:n.-559_-558dup
ENST00000359373.9:c.509+4438_509+4439dup	ENSP00000352332.5:n.509+4438_509+4439dup
ENST00000393609.7:c.509+4438_509+4439dup	ENSP00000377233.3:n.509+4438_509+4439dup
NM_001040118.2:c.509+4438_509+4439dup	NP_001035207.1:n.509+4438_509+4439dup
NM_001135190.1:c.-559_-558dup	NP_001128662.1:n.-559_-558dup
NM_015242.4:c.-559_-558dup	NP_056057.2:n.-559_-558dup
NM_001369489.1:c.-559_-558dup	NP_001356418.1:n.-559_-558dup
NR_161388.1:n.159_160dup
NM_001040118.3:c.509+4438_509+4439dup MANE Select	NP_001035207.1:n.509+4438_509+4439dup
NM_001135190.2:c.-559_-558dup	NP_001128662.1:n.-559_-558dup
NM_015242.5:c.-559_-558dup	NP_056057.2:n.-559_-558dup