Canonical Allele Identifier: CA2792663977

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72721718_72721719insT , CM000673.2:g.72721718_72721719insT	GRCh38
NC_000011.9:g.72432763_72432764insT , CM000673.1:g.72432763_72432764insT	GRCh37
NC_000011.8:g.72110411_72110412insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4901_509+4902insA MANE Select	ENSP00000377233.3:n.509+4901_509+4902insA
ENST00000334211.12:c.-227+131_-227+132insA	ENSP00000335506.8:n.-227+131_-227+132insA
ENST00000359373.9:c.509+4901_509+4902insA	ENSP00000352332.5:n.509+4901_509+4902insA
ENST00000393609.7:c.509+4901_509+4902insA	ENSP00000377233.3:n.509+4901_509+4902insA
ENST00000426523.5:c.-227+131_-227+132insA	ENSP00000392264.1:n.-227+131_-227+132insA
ENST00000429686.5:c.-227+131_-227+132insA	ENSP00000403127.1:n.-227+131_-227+132insA
ENST00000465814.5:n.239+131_239+132insA
NM_001040118.2:c.509+4901_509+4902insA	NP_001035207.1:n.509+4901_509+4902insA
NM_001135190.1:c.-227+131_-227+132insA	NP_001128662.1:n.-227+131_-227+132insA
NM_015242.4:c.-227+131_-227+132insA	NP_056057.2:n.-227+131_-227+132insA
NM_001369489.1:c.-227+131_-227+132insA	NP_001356418.1:n.-227+131_-227+132insA
NR_161388.1:n.491+131_491+132insA
NM_001040118.3:c.509+4901_509+4902insA MANE Select	NP_001035207.1:n.509+4901_509+4902insA
NM_001135190.2:c.-227+131_-227+132insA	NP_001128662.1:n.-227+131_-227+132insA
NM_015242.5:c.-227+131_-227+132insA	NP_056057.2:n.-227+131_-227+132insA