Canonical Allele Identifier: CA2614978199

Gene: ARAP1

Linked Data

• gnomAD v4: 11-72722030-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722030T>G , CM000673.2:g.72722030T>G	GRCh38
NC_000011.9:g.72433075T>G , CM000673.1:g.72433075T>G	GRCh37
NC_000011.8:g.72110723T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393609.8:c.509+4590A>C MANE Select	ENSP00000377233.3:n.509+4590A>C
ENST00000334211.12:c.-407A>C	ENSP00000335506.8:n.-407A>C
ENST00000359373.9:c.509+4590A>C	ENSP00000352332.5:n.509+4590A>C
ENST00000393609.7:c.509+4590A>C	ENSP00000377233.3:n.509+4590A>C
ENST00000465814.5:n.59A>C
NM_001040118.2:c.509+4590A>C	NP_001035207.1:n.509+4590A>C
NM_001135190.1:c.-407A>C	NP_001128662.1:n.-407A>C
NM_015242.4:c.-407A>C	NP_056057.2:n.-407A>C
NM_001369489.1:c.-407A>C	NP_001356418.1:n.-407A>C
NR_161388.1:n.311A>C
NM_001040118.3:c.509+4590A>C MANE Select	NP_001035207.1:n.509+4590A>C
NM_001135190.2:c.-407A>C	NP_001128662.1:n.-407A>C
NM_015242.5:c.-407A>C	NP_056057.2:n.-407A>C