Canonical Allele Identifier: CA1982116847

Gene: ARAP1

Linked Data

• dbSNP Id: rs1857538842
• gnomAD v4: 11-72722151-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722151C>G , CM000673.2:g.72722151C>G	GRCh38
NC_000011.9:g.72433196C>G , CM000673.1:g.72433196C>G	GRCh37
NC_000011.8:g.72110844C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4469G>C MANE Select	ENSP00000377233.3:n.509+4469G>C
ENST00000334211.12:c.-528G>C	ENSP00000335506.8:n.-528G>C
ENST00000359373.9:c.509+4469G>C	ENSP00000352332.5:n.509+4469G>C
ENST00000393609.7:c.509+4469G>C	ENSP00000377233.3:n.509+4469G>C
NM_001040118.2:c.509+4469G>C	NP_001035207.1:n.509+4469G>C
NM_001135190.1:c.-528G>C	NP_001128662.1:n.-528G>C
NM_015242.4:c.-528G>C	NP_056057.2:n.-528G>C
NM_001369489.1:c.-528G>C	NP_001356418.1:n.-528G>C
NR_161388.1:n.190G>C
NM_001040118.3:c.509+4469G>C MANE Select	NP_001035207.1:n.509+4469G>C
NM_001135190.2:c.-528G>C	NP_001128662.1:n.-528G>C
NM_015242.5:c.-528G>C	NP_056057.2:n.-528G>C