Canonical Allele Identifier: CA1982116853

Gene: ARAP1

Linked Data

• dbSNP Id: rs1857540221
• gnomAD v4: 11-72722154-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72722154A>G , CM000673.2:g.72722154A>G	GRCh38
NC_000011.9:g.72433199A>G , CM000673.1:g.72433199A>G	GRCh37
NC_000011.8:g.72110847A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.509+4466T>C MANE Select	ENSP00000377233.3:n.509+4466T>C
ENST00000334211.12:c.-531T>C	ENSP00000335506.8:n.-531T>C
ENST00000359373.9:c.509+4466T>C	ENSP00000352332.5:n.509+4466T>C
ENST00000393609.7:c.509+4466T>C	ENSP00000377233.3:n.509+4466T>C
NM_001040118.2:c.509+4466T>C	NP_001035207.1:n.509+4466T>C
NM_001135190.1:c.-531T>C	NP_001128662.1:n.-531T>C
NM_015242.4:c.-531T>C	NP_056057.2:n.-531T>C
NM_001369489.1:c.-531T>C	NP_001356418.1:n.-531T>C
NR_161388.1:n.187T>C
NM_001040118.3:c.509+4466T>C MANE Select	NP_001035207.1:n.509+4466T>C
NM_001135190.2:c.-531T>C	NP_001128662.1:n.-531T>C
NM_015242.5:c.-531T>C	NP_056057.2:n.-531T>C