Canonical Allele Identifier: CA1982116871

Gene: ARAP1

Linked Data

• dbSNP Id: rs1591225675
• gnomAD v4: 11-72722168-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722168A>G , CM000673.2:g.72722168A>G	GRCh38
NC_000011.9:g.72433213A>G , CM000673.1:g.72433213A>G	GRCh37
NC_000011.8:g.72110861A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4452T>C MANE Select	ENSP00000377233.3:n.509+4452T>C
ENST00000334211.12:c.-545T>C	ENSP00000335506.8:n.-545T>C
ENST00000359373.9:c.509+4452T>C	ENSP00000352332.5:n.509+4452T>C
ENST00000393609.7:c.509+4452T>C	ENSP00000377233.3:n.509+4452T>C
NM_001040118.2:c.509+4452T>C	NP_001035207.1:n.509+4452T>C
NM_001135190.1:c.-545T>C	NP_001128662.1:n.-545T>C
NM_015242.4:c.-545T>C	NP_056057.2:n.-545T>C
NM_001369489.1:c.-545T>C	NP_001356418.1:n.-545T>C
NR_161388.1:n.173T>C
NM_001040118.3:c.509+4452T>C MANE Select	NP_001035207.1:n.509+4452T>C
NM_001135190.2:c.-545T>C	NP_001128662.1:n.-545T>C
NM_015242.5:c.-545T>C	NP_056057.2:n.-545T>C