Canonical Allele Identifier: CA224448341
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs74506765

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72712967G>C , CM000673.2:g.72712967G>C GRCh38
NC_000011.9:g.72424012G>C , CM000673.1:g.72424012G>C GRCh37
NC_000011.8:g.72101660G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.747+209C>G MANE Select ENSP00000377233.3:p.=
ENST00000334211.12:c.12+209C>G ENSP00000335506.8:p.=
ENST00000359373.9:c.747+209C>G ENSP00000352332.5:p.=
ENST00000393605.7:c.-372C>G ENSP00000377230.3:p.=
ENST00000393609.7:c.747+209C>G ENSP00000377233.3:p.=
ENST00000426523.5:c.12+209C>G ENSP00000392264.1:p.=
ENST00000429686.5:c.12+209C>G ENSP00000403127.1:p.=
ENST00000465814.5:n.686C>G
NM_001040118.2:c.747+209C>G NP_001035207.1:p.=
NM_001135190.1:c.12+209C>G NP_001128662.1:p.=
NM_015242.4:c.12+209C>G NP_056057.2:p.=
NM_001369489.1:c.12+209C>G NP_001356418.1:p.=
NR_161388.1:n.729+209C>G
NM_001040118.3:c.747+209C>G MANE Select NP_001035207.1:p.=
NM_001135190.2:c.12+209C>G NP_001128662.1:p.=
NM_015242.5:c.12+209C>G NP_056057.2:p.=