Canonical Allele Identifier: CA224453194
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1056640723
MyVariant Identifiers: chr11:g.72722393C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722393C>G , CM000673.2:g.72722393C>G GRCh38
NC_000011.9:g.72433438C>G , CM000673.1:g.72433438C>G GRCh37
NC_000011.8:g.72111086C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4227G>C MANE Select ENSP00000377233.3:n.509+4227G>C
ENST00000359373.9:c.509+4227G>C ENSP00000352332.5:n.509+4227G>C
ENST00000393609.7:c.509+4227G>C ENSP00000377233.3:n.509+4227G>C
NM_001040118.2:c.509+4227G>C NP_001035207.1:n.509+4227G>C
NM_001040118.3:c.509+4227G>C MANE Select NP_001035207.1:n.509+4227G>C
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