Canonical Allele Identifier: CA1982116681

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72721827_72721836delinsAGCAACGGCG , CM000673.2:g.72721827_72721836delinsAGCAACGGCG	GRCh38
NC_000011.9:g.72432872_72432881delinsAGCAACGGCG , CM000673.1:g.72432872_72432881delinsAGCAACGGCG	GRCh37
NC_000011.8:g.72110520_72110529delinsAGCAACGGCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4784_509+4793delinsCGCCGTTGCT MANE Select	ENSP00000377233.3:n.509+4784_509+4793delinsCGCCGTTGCT
ENST00000334211.12:c.-227+14_-227+23delinsCGCCGTTGCT	ENSP00000335506.8:n.-227+14_-227+23delinsCGCCGTTGCT
ENST00000359373.9:c.509+4784_509+4793delinsCGCCGTTGCT	ENSP00000352332.5:n.509+4784_509+4793delinsCGCCGTTGCT
ENST00000393609.7:c.509+4784_509+4793delinsCGCCGTTGCT	ENSP00000377233.3:n.509+4784_509+4793delinsCGCCGTTGCT
ENST00000426523.5:c.-227+14_-227+23delinsCGCCGTTGCT	ENSP00000392264.1:n.-227+14_-227+23delinsCGCCGTTGCT
ENST00000429686.5:c.-227+14_-227+23delinsCGCCGTTGCT	ENSP00000403127.1:n.-227+14_-227+23delinsCGCCGTTGCT
ENST00000465814.5:n.239+14_239+23delinsCGCCGTTGCT
NM_001040118.2:c.509+4784_509+4793delinsCGCCGTTGCT	NP_001035207.1:n.509+4784_509+4793delinsCGCCGTTGCT
NM_001135190.1:c.-227+14_-227+23delinsCGCCGTTGCT	NP_001128662.1:n.-227+14_-227+23delinsCGCCGTTGCT
NM_015242.4:c.-227+14_-227+23delinsCGCCGTTGCT	NP_056057.2:n.-227+14_-227+23delinsCGCCGTTGCT
NM_001369489.1:c.-227+14_-227+23delinsCGCCGTTGCT	NP_001356418.1:n.-227+14_-227+23delinsCGCCGTTGCT
NR_161388.1:n.491+14_491+23delinsCGCCGTTGCT
NM_001040118.3:c.509+4784_509+4793delinsCGCCGTTGCT MANE Select	NP_001035207.1:n.509+4784_509+4793delinsCGCCGTTGCT
NM_001135190.2:c.-227+14_-227+23delinsCGCCGTTGCT	NP_001128662.1:n.-227+14_-227+23delinsCGCCGTTGCT
NM_015242.5:c.-227+14_-227+23delinsCGCCGTTGCT	NP_056057.2:n.-227+14_-227+23delinsCGCCGTTGCT