Canonical Allele Identifier: CA224453103
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs892097203

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722084A>G , CM000673.2:g.72722084A>G GRCh38
NC_000011.9:g.72433129A>G , CM000673.1:g.72433129A>G GRCh37
NC_000011.8:g.72110777A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4536T>C MANE Select ENSP00000377233.3:n.509+4536T>C
ENST00000334211.12:c.-461T>C ENSP00000335506.8:n.-461T>C
ENST00000359373.9:c.509+4536T>C ENSP00000352332.5:n.509+4536T>C
ENST00000393609.7:c.509+4536T>C ENSP00000377233.3:n.509+4536T>C
ENST00000465814.5:n.5T>C
NM_001040118.2:c.509+4536T>C NP_001035207.1:n.509+4536T>C
NM_001135190.1:c.-461T>C NP_001128662.1:n.-461T>C
NM_015242.4:c.-461T>C NP_056057.2:n.-461T>C
NM_001369489.1:c.-461T>C NP_001356418.1:n.-461T>C
NR_161388.1:n.257T>C
NM_001040118.3:c.509+4536T>C MANE Select NP_001035207.1:n.509+4536T>C
NM_001135190.2:c.-461T>C NP_001128662.1:n.-461T>C
NM_015242.5:c.-461T>C NP_056057.2:n.-461T>C