Canonical Allele Identifier: CA679994298
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1214676207

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722048T>C , CM000673.2:g.72722048T>C GRCh38
NC_000011.9:g.72433093T>C , CM000673.1:g.72433093T>C GRCh37
NC_000011.8:g.72110741T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4572A>G MANE Select ENSP00000377233.3:n.509+4572A>G
ENST00000334211.12:c.-425A>G ENSP00000335506.8:n.-425A>G
ENST00000359373.9:c.509+4572A>G ENSP00000352332.5:n.509+4572A>G
ENST00000393609.7:c.509+4572A>G ENSP00000377233.3:n.509+4572A>G
ENST00000465814.5:n.41A>G
NM_001040118.2:c.509+4572A>G NP_001035207.1:n.509+4572A>G
NM_001135190.1:c.-425A>G NP_001128662.1:n.-425A>G
NM_015242.4:c.-425A>G NP_056057.2:n.-425A>G
NM_001369489.1:c.-425A>G NP_001356418.1:n.-425A>G
NR_161388.1:n.293A>G
NM_001040118.3:c.509+4572A>G MANE Select NP_001035207.1:n.509+4572A>G
NM_001135190.2:c.-425A>G NP_001128662.1:n.-425A>G
NM_015242.5:c.-425A>G NP_056057.2:n.-425A>G