Canonical Allele Identifier: CA2792664016
Gene: ARAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722513C>T , CM000673.2:g.72722513C>T GRCh38
NC_000011.9:g.72433558C>T , CM000673.1:g.72433558C>T GRCh37
NC_000011.8:g.72111206C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4107G>A MANE Select ENSP00000377233.3:n.509+4107G>A
ENST00000359373.9:c.509+4107G>A ENSP00000352332.5:n.509+4107G>A
ENST00000393609.7:c.509+4107G>A ENSP00000377233.3:n.509+4107G>A
NM_001040118.2:c.509+4107G>A NP_001035207.1:n.509+4107G>A
NM_001040118.3:c.509+4107G>A MANE Select NP_001035207.1:n.509+4107G>A
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