Canonical Allele Identifier: CA224448256

Gene: ARAP1

Linked Data

• dbSNP Id: rs113515643
• gnomAD v4: 11-72712606-A-C
• MyVariant Identifiers: chr11:g.72423651A>C (hg19) ; chr11:g.72712606A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72712606A>C , CM000673.2:g.72712606A>C	GRCh38
NC_000011.9:g.72423651A>C , CM000673.1:g.72423651A>C	GRCh37
NC_000011.8:g.72101299A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393609.8:c.748-38T>G MANE Select	ENSP00000377233.3:n.748-38T>G
ENST00000334211.12:c.13-38T>G	ENSP00000335506.8:n.13-38T>G
ENST00000359373.9:c.748-38T>G	ENSP00000352332.5:n.748-38T>G
ENST00000393605.7:c.-11T>G	ENSP00000377230.3:n.-11T>G
ENST00000393609.7:c.748-38T>G	ENSP00000377233.3:n.748-38T>G
ENST00000426523.5:c.13-38T>G	ENSP00000392264.1:n.13-38T>G
ENST00000429686.5:c.13-38T>G	ENSP00000403127.1:n.13-38T>G
ENST00000465814.5:n.1047T>G
NM_001040118.2:c.748-38T>G	NP_001035207.1:n.748-38T>G
NM_001135190.1:c.13-38T>G	NP_001128662.1:n.13-38T>G
NM_015242.4:c.13-38T>G	NP_056057.2:n.13-38T>G
NM_001369489.1:c.13-38T>G	NP_001356418.1:n.13-38T>G
NR_161388.1:n.730-38T>G
NM_001040118.3:c.748-38T>G MANE Select	NP_001035207.1:n.748-38T>G
NM_001135190.2:c.13-38T>G	NP_001128662.1:n.13-38T>G
NM_015242.5:c.13-38T>G	NP_056057.2:n.13-38T>G