Canonical Allele Identifier: CA1982116813

Gene: ARAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722052_72722053delinsCA , CM000673.2:g.72722052_72722053delinsCA	GRCh38
NC_000011.9:g.72433097_72433098delinsCA , CM000673.1:g.72433097_72433098delinsCA	GRCh37
NC_000011.8:g.72110745_72110746delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4567_509+4568delinsTG MANE Select	ENSP00000377233.3:n.509+4567_509+4568delinsTG
ENST00000334211.12:c.-430_-429delinsTG	ENSP00000335506.8:n.-430_-429delinsTG
ENST00000359373.9:c.509+4567_509+4568delinsTG	ENSP00000352332.5:n.509+4567_509+4568delinsTG
ENST00000393609.7:c.509+4567_509+4568delinsTG	ENSP00000377233.3:n.509+4567_509+4568delinsTG
ENST00000465814.5:n.36_37delinsTG
NM_001040118.2:c.509+4567_509+4568delinsTG	NP_001035207.1:n.509+4567_509+4568delinsTG
NM_001135190.1:c.-430_-429delinsTG	NP_001128662.1:n.-430_-429delinsTG
NM_015242.4:c.-430_-429delinsTG	NP_056057.2:n.-430_-429delinsTG
NM_001369489.1:c.-430_-429delinsTG	NP_001356418.1:n.-430_-429delinsTG
NR_161388.1:n.288_289delinsTG
NM_001040118.3:c.509+4567_509+4568delinsTG MANE Select	NP_001035207.1:n.509+4567_509+4568delinsTG
NM_001135190.2:c.-430_-429delinsTG	NP_001128662.1:n.-430_-429delinsTG
NM_015242.5:c.-430_-429delinsTG	NP_056057.2:n.-430_-429delinsTG