Canonical Allele Identifier: CA224453093
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs916300994

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722014C>T , CM000673.2:g.72722014C>T GRCh38
NC_000011.9:g.72433059C>T , CM000673.1:g.72433059C>T GRCh37
NC_000011.8:g.72110707C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4606G>A MANE Select ENSP00000377233.3:n.509+4606G>A
ENST00000334211.12:c.-391G>A ENSP00000335506.8:n.-391G>A
ENST00000359373.9:c.509+4606G>A ENSP00000352332.5:n.509+4606G>A
ENST00000393609.7:c.509+4606G>A ENSP00000377233.3:n.509+4606G>A
ENST00000426523.5:c.-391G>A ENSP00000392264.1:n.-391G>A
ENST00000429686.5:c.-391G>A ENSP00000403127.1:n.-391G>A
ENST00000465814.5:n.75G>A
NM_001040118.2:c.509+4606G>A NP_001035207.1:n.509+4606G>A
NM_001135190.1:c.-391G>A NP_001128662.1:n.-391G>A
NM_015242.4:c.-391G>A NP_056057.2:n.-391G>A
NM_001369489.1:c.-391G>A NP_001356418.1:n.-391G>A
NR_161388.1:n.327G>A
NM_001040118.3:c.509+4606G>A MANE Select NP_001035207.1:n.509+4606G>A
NM_001135190.2:c.-391G>A NP_001128662.1:n.-391G>A
NM_015242.5:c.-391G>A NP_056057.2:n.-391G>A