Canonical Allele Identifier: CA679994270
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1265789367

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72722020C>T , CM000673.2:g.72722020C>T GRCh38
NC_000011.9:g.72433065C>T , CM000673.1:g.72433065C>T GRCh37
NC_000011.8:g.72110713C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393609.8:c.509+4600G>A MANE Select ENSP00000377233.3:n.509+4600G>A
ENST00000334211.12:c.-397G>A ENSP00000335506.8:n.-397G>A
ENST00000359373.9:c.509+4600G>A ENSP00000352332.5:n.509+4600G>A
ENST00000393609.7:c.509+4600G>A ENSP00000377233.3:n.509+4600G>A
ENST00000426523.5:c.-397G>A ENSP00000392264.1:n.-397G>A
ENST00000429686.5:c.-397G>A ENSP00000403127.1:n.-397G>A
ENST00000465814.5:n.69G>A
NM_001040118.2:c.509+4600G>A NP_001035207.1:n.509+4600G>A
NM_001135190.1:c.-397G>A NP_001128662.1:n.-397G>A
NM_015242.4:c.-397G>A NP_056057.2:n.-397G>A
NM_001369489.1:c.-397G>A NP_001356418.1:n.-397G>A
NR_161388.1:n.321G>A
NM_001040118.3:c.509+4600G>A MANE Select NP_001035207.1:n.509+4600G>A
NM_001135190.2:c.-397G>A NP_001128662.1:n.-397G>A
NM_015242.5:c.-397G>A NP_056057.2:n.-397G>A