Canonical Allele Identifier: CA1982116858

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722158_72722182delinsAGAGAGAGAGAGAGAAAGACAGAGG , CM000673.2:g.72722158_72722182delinsAGAGAGAGAGAGAGAAAGACAGAGG	GRCh38
NC_000011.9:g.72433203_72433227delinsAGAGAGAGAGAGAGAAAGACAGAGG , CM000673.1:g.72433203_72433227delinsAGAGAGAGAGAGAGAAAGACAGAGG	GRCh37
NC_000011.8:g.72110851_72110875delinsAGAGAGAGAGAGAGAAAGACAGAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCTCTCT MANE Select	ENSP00000377233.3:n.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTC...
ENST00000334211.12:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	ENSP00000335506.8:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT
ENST00000359373.9:c.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCTCTCT	ENSP00000352332.5:n.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTC...
ENST00000393609.7:c.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCTCTCT	ENSP00000377233.3:n.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTC...
NM_001040118.2:c.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_001035207.1:n.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCT...
NM_001135190.1:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_001128662.1:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT
NM_015242.4:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_056057.2:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT
NM_001369489.1:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_001356418.1:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT
NR_161388.1:n.159_183delinsCCTCTGTCTTTCTCTCTCTCTCTCT
NM_001040118.3:c.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCTCTCT MANE Select	NP_001035207.1:n.509+4438_509+4462delinsCCTCTGTCTTTCTCTCTCTCT...
NM_001135190.2:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_001128662.1:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT
NM_015242.5:c.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT	NP_056057.2:n.-559_-535delinsCCTCTGTCTTTCTCTCTCTCTCTCT