Canonical Allele Identifier: CA1982116913

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722208_72722209delinsTG , CM000673.2:g.72722208_72722209delinsTG	GRCh38
NC_000011.9:g.72433253_72433254delinsTG , CM000673.1:g.72433253_72433254delinsTG	GRCh37
NC_000011.8:g.72110901_72110902delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4411_509+4412delinsCA MANE Select	ENSP00000377233.3:n.509+4411_509+4412delinsCA
ENST00000334211.12:c.-586_-585delinsCA	ENSP00000335506.8:n.-586_-585delinsCA
ENST00000359373.9:c.509+4411_509+4412delinsCA	ENSP00000352332.5:n.509+4411_509+4412delinsCA
ENST00000393609.7:c.509+4411_509+4412delinsCA	ENSP00000377233.3:n.509+4411_509+4412delinsCA
NM_001040118.2:c.509+4411_509+4412delinsCA	NP_001035207.1:n.509+4411_509+4412delinsCA
NM_001135190.1:c.-586_-585delinsCA	NP_001128662.1:n.-586_-585delinsCA
NM_015242.4:c.-586_-585delinsCA	NP_056057.2:n.-586_-585delinsCA
NM_001369489.1:c.-586_-585delinsCA	NP_001356418.1:n.-586_-585delinsCA
NR_161388.1:n.132_133delinsCA
NM_001040118.3:c.509+4411_509+4412delinsCA MANE Select	NP_001035207.1:n.509+4411_509+4412delinsCA
NM_001135190.2:c.-586_-585delinsCA	NP_001128662.1:n.-586_-585delinsCA
NM_015242.5:c.-586_-585delinsCA	NP_056057.2:n.-586_-585delinsCA