Canonical Allele Identifier: CA939468437
Gene: ARAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1857525805

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72721886_72721889dup , CM000673.2:g.72721886_72721889dup GRCh38
NC_000011.9:g.72432931_72432934dup , CM000673.1:g.72432931_72432934dup GRCh37
NC_000011.8:g.72110579_72110582dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393609.8:c.509+4732_509+4735dup MANE Select ENSP00000377233.3:n.509+4732_509+4735dup
ENST00000334211.12:c.-265_-262dup ENSP00000335506.8:n.-265_-262dup
ENST00000359373.9:c.509+4732_509+4735dup ENSP00000352332.5:n.509+4732_509+4735dup
ENST00000393609.7:c.509+4732_509+4735dup ENSP00000377233.3:n.509+4732_509+4735dup
ENST00000426523.5:c.-265_-262dup ENSP00000392264.1:n.-265_-262dup
ENST00000429686.5:c.-265_-262dup ENSP00000403127.1:n.-265_-262dup
ENST00000465814.5:n.201_204dup
NM_001040118.2:c.509+4732_509+4735dup NP_001035207.1:n.509+4732_509+4735dup
NM_001135190.1:c.-265_-262dup NP_001128662.1:n.-265_-262dup
NM_015242.4:c.-265_-262dup NP_056057.2:n.-265_-262dup
NM_001369489.1:c.-265_-262dup NP_001356418.1:n.-265_-262dup
NR_161388.1:n.453_456dup
NM_001040118.3:c.509+4732_509+4735dup MANE Select NP_001035207.1:n.509+4732_509+4735dup
NM_001135190.2:c.-265_-262dup NP_001128662.1:n.-265_-262dup
NM_015242.5:c.-265_-262dup NP_056057.2:n.-265_-262dup