Canonical Allele Identifier: CA1982116832
Gene: ARAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722100_72722102delinsCGT , CM000673.2:g.72722100_72722102delinsCGT GRCh38
NC_000011.9:g.72433145_72433147delinsCGT , CM000673.1:g.72433145_72433147delinsCGT GRCh37
NC_000011.8:g.72110793_72110795delinsCGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4518_509+4520delinsACG MANE Select ENSP00000377233.3:n.509+4518_509+4520deli...
ENST00000334211.12:c.-479_-477delinsACG ENSP00000335506.8:n.-479_-477delinsACG
ENST00000359373.9:c.509+4518_509+4520delinsACG ENSP00000352332.5:n.509+4518_509+4520deli...
ENST00000393609.7:c.509+4518_509+4520delinsACG ENSP00000377233.3:n.509+4518_509+4520deli...
NM_001040118.2:c.509+4518_509+4520delinsACG NP_001035207.1:n.509+4518_509+4520delinsA...
NM_001135190.1:c.-479_-477delinsACG NP_001128662.1:n.-479_-477delinsACG
NM_015242.4:c.-479_-477delinsACG NP_056057.2:n.-479_-477delinsACG
NM_001369489.1:c.-479_-477delinsACG NP_001356418.1:n.-479_-477delinsACG
NR_161388.1:n.239_241delinsACG
NM_001040118.3:c.509+4518_509+4520delinsACG MANE Select NP_001035207.1:n.509+4518_509+4520delinsA...
NM_001135190.2:c.-479_-477delinsACG NP_001128662.1:n.-479_-477delinsACG
NM_015242.5:c.-479_-477delinsACG NP_056057.2:n.-479_-477delinsACG